Page 1


HumPCRTM ACT.ISR Detection Kit 2. SPECIMEN

Pus, tissue, or other material properly obtained from an abscess, biopsy, aspirate, drainage, exudate, lesion, or wound. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Actinomyces israelii is a strict anaerobic, Gram-positive, non-motile, branching filamentous bacterium. The organism is a common saprophyte of the oropharynx and the gastrointestinal tract. Since they have not been recovered from other natural habitats, infections are believed to be endogenous. Actinomycosis is an infection primarily caused by A. israelii. This disease is a chronic suppurative and granulomatous infection that produces pyogenic lesions with local or systemic manifestations. Based on the site of involment, the most common are cervicofacial, thoracic and abdominal actinomycosis. Infections can occur in all age groups and the main predisposing factors are a local trauma such dental extraction or broken bone. HumPCR™ ACT.ISR Detection Kit is the direct detection of Actinomyces israelii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Expected PCR product size : 453 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM ACT.ISR Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : ACT.ISR Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM ACT.ISR Molecular Diagnostic

Catalog No. HUM0001(S)

HumPCRTM ACT.ISR Detection Kit 48 or 96

HUM0001(48) HUM0001(96)

BrigTM Molecular Weight Marker

HUMAN

453 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BKV Detection Kit 2. SPECIMEN

Urine, serum, plasma, whole blood, or cerebrospinal fluid (CSF) 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

The Polyomavirus are members of the papovavirus family. They are double stranded DNA virus and are widely distributed among various animal species. The Polyomavirus includes the BK virus (BKV) that naturally infects humans. Seroprevalence studies have shown that BKV infection is widespread in children throughout the world, and the virus thereafter persists latently in the kidney for life. Althought in inmunocompetent individuals BK infection is generally asymptomatic, lowering of immunity can occasionally result in life-threatening renal disease. HumPCR™ BKV Detection Kit is the direct detection of BK virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 374 bp M

P

1

2

3

N

400bp

374 bp

Fig1. Electrophoresis of PCR product by VetPCRTM BKV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : BKV Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BKV Molecular Diagnostic

Catalog No. HUM0008(S)

HumPCRTM BKV Detection Kit 48 or 96

HUM0008(48) HUM0008(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BOR.AF Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), blood, or synovial fluid. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Bacterial infection with specific spirochetes from the genus Borrelia, usually acquired from the bite of an infected Ixodes tick, is the causative agent of Lyme disease (LD). LD is the most common tick-borne disease in the northern hemisphere, producing a wide range of disabling effects on multiple human targets, including the skin, the nervous system, the joints and the heart. The species complex B. burgdorferi is predominantly responsible for LD cases in the United States while B. burgdorferi, B. afzelii and B. garinii are the responsible pathogenic species in Europe and Asia. Presentation and destructive effects of LD vary widely depending on the stage and magnitude of spirochete dissemination. Initial effects may include rashes or flu-like symptoms, while later stages may be characterized by arthritic, neurological, psychiatric and cardiac symptoms. HumPCRTM BOR.AF Detection Kit is the direct detection of Borrelia afzelii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 540 bp M

1

2

3

P

N

600bp

Fig1. Electrophoresis of PCR product by VetPCRTM BOR.AF Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : BOR.AF Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BOR.AF Molecular Diagnostic

Catalog No. HUM0009(S)

HumPCRTM BOR.AF Detection Kit 48 or 96

HUM0009(48) HUM0009(96)

BrigTM Molecular Weight Marker

HUMAN

540 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BOR.BURG Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), blood, or synovial fluid. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Bacterial infection with specific spirochetes from the genus Borrelia, usually acquired from the bite of an infected Ixodes tick, is the causative agent of Lyme disease (LD). LD is the most common tick-borne disease in the northern hemisphere, producing a wide range of disabling effects on multiple human targets, including the skin, the nervous system, the joints and the heart. The species complex B. burgdorferi is predominantly responsible for LD cases in the United States while B. burgdorferi, B. afzelii and B. garinii are the responsible pathogenic species in Europe and Asia. Presentation and destructive effects of LD vary widely depending on the stage and magnitude of spirochete dissemination. Initial effects may include rashes or flu-like symptoms, while later stages may be characterized by arthritic, neurological, psychiatric and cardiac symptoms. HumPCRTM BOR.BURG Detection Kit is the direct detection of Borrelia burgdorferi on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 452 bp M

N

1

2

3

P

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM BOR.BURG Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : BOR.BURG Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM BOR.BURG Molecular Diagnostic

Catalog No. HUM0010(S)

HumPCRTM BOR.BURG Detection Kit 48 or 96

HUM0010(48) HUM0010(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BOR.GAR Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), blood, or synovial fluid. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Bacterial infection with specific spirochetes from the genus Borrelia, usually acquired from the bite of an infected Ixodes tick, is the causative agent of Lyme disease (LD). LD is the most common tick-borne disease in the northern hemisphere, producing a wide range of disabling effects on multiple human targets, including the skin, the nervous system, the joints and the heart. The species complex B. burgdorferi is predominantly responsible for LD cases in the United States while B. burgdorferi, B. afzelii and B. garinii are the responsible pathogenic species in Europe and Asia. Presentation and destructive effects of LD vary widely depending on the stage and magnitude of spirochete dissemination. Initial effects may include rashes or flu-like symptoms, while later stages may be characterized by arthritic, neurological, psychiatric and cardiac symptoms. HumPCRTM BOR.GAR Detection Kit is the direct detection of Borrelia garinii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 225 bp M

P

1

2

3

N

200bp

Fig1. Electrophoresis of PCR product by VetPCRTM BOR.GAR Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : BOR.GAR Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BOR.GAR Molecular Diagnostic

Catalog No. HUM0011(S)

HumPCRTM BOR.GAR Detection Kit 48 or 96

HUM0011(48) HUM0011(96)

BrigTM Molecular Weight Marker

HUMAN

225 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BOR.PERTU Detection Kit 2. SPECIMEN

Nasopharyngeal swab, wash or aspirate, sputum. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Bordetella Pertussis is a Gram-negative, aerobic, non motile coccobacillus and the causative agent of pertussis or whooping cough, an acute infectious illness of the respiratory tract. This disease remains endemic in developed nations despite high vaccination coverage. Worldwide, there are an estimated 50 million cases occurring annually, 90% of which are in developing countries. There are over 400,0000 pertussis-related deaths. The bacterium spreads very easily in droplets produced by coughing or sneezing. The initial symptoms, very similar to the common cold, usually develop about a week after exposure to the bacteria. Severe episodes of coughing start about 10 to 12 days later. The infection usually lasts 6 weeks. Treatment with an antibiotic, usually erythromycin, clarithromycin or azithromycin may make the illness less severe. HumPCR™ BOR.PERTU Detection Kit is the direct detection of Bordetella Pertussis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 343 bp M

P

1

2

3

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM BOR.PERTU Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : BOR.PERTU Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BOR.PERTU Molecular Diagnostic

Catalog No. HUM0012(S)

HumPCRTM BOR.PERTU Detection Kit 48 or 96

HUM0012(48) HUM0012(96)

BrigTM Molecular Weight Marker

HUMAN

343 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BOR.PPERTU Detection Kit 2. SPECIMEN

Nasopharyngeal swab, wash or aspirate, sputum. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Bordetella Parapertussis is a Gram-negative, aerobic coccobacillus and the causative agent for a whooping cough-like disease. Generally has a milder clinical presentation, but it is not easily distinguished from B. pertussis infection by symptoms. The bacterium spreads very easily in droplets produced by coughing or sneezing. The incubation period is five to 10 days. At first, the infected person appears to have a common cold with runny nose, watery eyes, sneezing, fever, and a mild cough. More severe episodes of coughing start about 10 to 12 days later. Treatment with an antibiotic, usually erythromycin, clarithromycin or azithromycin may make the illness less severe. HumPCR™ BOR.PPERTU Detection Kit is the direct detection of Bordetella Parapertussis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 486 bp M

N

P

1

2

3

4

486 bp

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM BOR.PPERTU Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~4 : BOR.PPERTU Positive sample 4. ORDERING INFORMATION Product HumPCRTM BOR.PPERTU Molecular Diagnostic

Catalog No. HUM0013(S)

HumPCRTM BOR.PPERTU Detection Kit 48 or 96

HUM0013(48) HUM0013(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BRU.AB Detection Kit 2. SPECIMEN 1. DESCRIPTION

Whole blood, bone marrow, CSF. 3. INTERPRETATION OF RESULTS

Brucella species are facultative intracellular, gram-negative coccobacilli. Brucellosis is a zoonosis transmitted to humans from infected animals. Brucella abortus affects mainly cattle. Dairy products prepared from unpasteurized milk such as soft cheese, yoghurts and ice-creams may contain high concentration of the bacteria and consumption of these is an important cause of brucellosis. Symptoms of brucellosis can be very diverse depending on the site of infection and include encephalitis, meningitis, spondylitis, arthritis, endocarditis, orchitis, and prostatitis. Lack of appropriate therapy during the acute phase may result in localization of brucellae in various tissues and organs and lead to subacute or chronic disease that is very hard to treat. Accurate and fast diagnosis of human brucellosis is very important as delay or misdiagnosis usually results in treatment failures, relapses, chronic courses, focal complications, and a high case-fatality rate. Hum PCRTM BRU.AB Detection Kit is the direct detection of Brucella abortus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 322 bp M

P

1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM BRU.AB Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : BRU.AB Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BRU.AB Molecular Diagnostic

Catalog No. HUM0015(S)

HumPCRTM BRU.AB Detection Kit 48 or 96

HUM0015(48) HUM0015(96)

BrigTM Molecular Weight Marker

HUMAN

322 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM BRU.CANIS Detection Kit 2. SPECIMEN 1. DESCRIPTION

Whole blood, bone marrow, CSF. 3. INTERPRETATION OF RESULTS

Brucella canis is a Gram-negative, aerobic, intracellular coccobacillus. Human infections with B. canis are much less commonly diagnosed than those caused by other Brucella species, consequently the true incidence of human brucellosis is unknown. Reported incidence in endemic-disease areas varies widely. Dogs are the only natural reservoir of the organism. The transmission of Brucella canis to man commonly occurs through contact with infected dogs or their secretions. The clinical features of brucellosis depend on the stage of the disease, and the organs and systems involved. Typically, brucellosis begins as an acute febrile illness with nonspecific flu-like signs such as fever, headache, malaise, back pain, myalgia and generalized aches. The timely and accurate diagnosis of human brucellosis continues to challenge clinicians because of its non-specific clinical features, slow growth rate in blood cultures, and the complexity of its serodiagnosis. HumPCRTM BRU.CANIS Detection Kit is the direct detection of Brucella canis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 322 bp M

P

1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM BRU.CANIS Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : BRU.CANIS Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM BRU.CANIS Molecular Diagnostic

Catalog No. HUM0016(S)

HumPCRTM BRU.CANIS Detection Kit 48 or 96

HUM0016(48) HUM0016(96)

BrigTM Molecular Weight Marker

HUMAN

322 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CAN.ALB Detection Kit 2. SPECIMEN 1. DESCRIPTION

Candida albicans is a dimorphic yeast and a common member of he oropharyngeal, gastrointestinal, and female genital flora in about 80% of the individuals, but does not usually colonize normal skin. Infections occur when competing bacterial flora are eliminated, for example, by antibacterial antibiotics, allowing the yeast to overgrow. C. albicans is the most prevalent human fungal pathogen. Infections have various manifestations depending of the site: oral and vaginal candidiasis s common in HIV-infected individuals; systemic candidiasis is a life-threatening infection that can involve the gastrointestinal tract, kidneys, liver and spleen. Direct microscopy of skin or mucous membranes scrapings, histological methods and growth on Sabouraud agar are the most used techniques for the diagnosis of candidiasis. HumPCR™ CAN.ALB Detection Kit is the direct detection of Candida albicans on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Whole blood, biopsy, body fluid, aspirates, bronchoalveolar lavage (BAL), swab of conjunctiva, skin, nails, hair, sputum, stool, throat, tissue, urine, or vaginal. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 317 bp M P 1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM CAN.ALB Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : CAN.ALB Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CAN.ALB Molecular Diagnostic

Catalog No. HUM0018(S)

HumPCRTM CAN.ALB Detection Kit 48 or 96

HUM0018(48) HUM0018(96)

BrigTM Molecular Weight Marker

HUMAN

317 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CAN.GLA Detection Kit 1. DESCRIPTION

2. SPECIMEN Whole blood, biopsy, body fluid, aspirates, bronchoalveolar lavage (BAL), swab of conjunctiva, skin, nails, hair, sputum, stool, throat, tissue, urine, or vaginal. 3. INTERPRETATION OF RESULTS

Candida species are ubiquitous fungi that represent the most common opportunistic fungal pathogens in humans, with Candida albicans being the most prevalent pathogen in mucosal and systemic fungal infections. Candida glabrata has been considered a relative nonpathogenic saprophyte of the normal flora of healthy individuals, rarely causing serious infections in humans. However, as a consequence of the widespread use of immunosuppressive drugs and the emergence of the acquired immunodeficiency syndrome (AIDS), the frequency of mucosal and systemic infections caused by C. glabrata has increased signiďŹ cantly. Oral candidiasis is a common opportunistic infection in immunocompromised populations. C. glabrata has emerged as a notable pathogenic agent in the oral mucosa, either as a co-infecting agent with C. albicans or as the sole detectable species from oral lesions. C. glabrata is extremely difficult to treat and is associated with systemic infections having a high mortality rate. HumPCR™ CAN.GLA Detection Kit is the direct detection of Candida glabrata on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 295 bp M

1

2

3

P

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM CAN.GLA Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : CAN.GLA Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CAN.GLA Molecular Diagnostic

Catalog No. HUM0019(S)

HumPCRTM CAN.GLA Detection Kit 48 or 96

HUM0019(48) HUM0019(96)

BrigTM Molecular Weight Marker

HUMAN

295 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CAN.spp Detection Kit 2. SPECIMEN 1. DESCRIPTION

Candida organisms are small, thin-walled, ovoid cells that reproduce by budding. Candida is used to refer to more than 100 fungal species, but only a small number are humans pathogens. Candida species are saprophytic eukaryotic organisms, spending much of their life as commensals of the gastrointestinal tract and mucous membranes of humans but it can become manifest as a pathogen in people with compromised defense mechanisms. Other risks factors include use of broad-spectrum antibiotics, renal failure requiring dialysis, central intravenous catheters and parenteral nutrition. The spectrum of infection varies from superficial candidiasis affecting the skin and mucosae to systemic infections where multiple organs may be affected. Most infections are endogenous, that is, they are the result of the individual’s own organisms rather than acquired from an outside source. The diagnosis includes histopathological evidence of infection and culturing of the organism. HumPCR™ CAN.SPP Detection Kit is the direct detection of Candida spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Whole blood, biopsy, body fluid, aspirates, bronchoalveolar lavage (BAL), swab of conjunctiva, skin, nails, hair, sputum, stool, throat, tissue, urine, or vaginal. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 171 bp M

N

P

1

2

3

200bp

Fig1. Electrophoresis of PCR product by VetPCRTM CAN.spp Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~3 : CAN.spp Positive sample 4. ORDERING INFORMATION Product HumPCRTM CAN.spp Molecular Diagnostic

Catalog No. HUM0020(S)

HumPCRTM CAN.spp Detection Kit 48 or 96

HUM0020(48) HUM0020(96)

BrigTM Molecular Weight Marker

HUMAN

171 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CHLA.NEUMO Detection Kit 2. SPECIMEN 1. DESCRIPTION

Respiratory (nasopharyngeal, sputum, and throat) clinical specimens. 3. INTERPRETATION OF RESULTS

Chlamydia pneumoniae is a Gram-negative obligate intracellular bacterium with a biphasic development cycle in which they alternate between the infectious extracellular and metabolically inactive form (the elementary body) and the intracellular, metabollicaly active replicating form (the reticulate body). Chlamydia pneumoniae is a common cause of upper respiratory tracts infections and has been associated with other acute and chronic respiratory diseases such as otitis media and chronic obstructive pulmonary disease. The clinical spectrum of C. pneumoniae infection has been extended to atherosclerosis, a major cause of cardiovascular disease and death in the western world. The incubation period is approximately 3-4 weeks. Symptoms of bronchitis or pneumonia follow upper respiratory tract symptoms (rhinitis, laryngitis, pharyngitis, sinusitis) in 1-4 weeks. Coinfection with other pathogens, especially M. pneumoniae and S. pneumoniae, can be frequent. C. pneumoniae is susceptible to macrolides, tetracyclines, and quinolones, but is resistant to sulfonamides. HumPCR™ CHLA. NEUMO Detection Kit is the direct detection of Chlamydia pneumoniae on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 193 bp M

1

2

3

P

N

200bp

Fig1. Electrophoresis of PCR product by VetPCRTM CHLA.NEUMO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : CHLA.NEUMO Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CHLA.NEUMO Molecular Diagnostic

Catalog No. HUM0021(S)

HumPCRTM CHLA.NEUMO Detection Kit 48 or 96

HUM0021(48) HUM0021(96)

BrigTM Molecular Weight Marker

HUMAN

193 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CHLA.PSI Detection Kit 2. SPECIMEN

Lung/bronchial washings or lung biopsy, node aspirates. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Chlamydophila psittaci is an obligate intracellular pathogen of both mammals and birds. This organism relies on their hosts for energy and nutrients. Chlamydophila receive nucleotides, lipids, and amino acids from their hosts. C. psittaci can infect humans through inhalation of contaminated aerosols from urine, respiratory and eye secretions, or dried faeces from a diseased animal or asymptomatic carrier. Psittacosis in humans is considered a rare but potentially severe and life-threatening disease characterized by flulike symptoms at the initial stage, such as headache, fever, listlessness and anorexia. In the absence of early antibiotic therapy, the infection can take a protracted course with the possibility of a fatal outcome. HumPCRTM CHLA.PSI Detection Kit is the direct detection of Chlamydophila psittaci on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 271 bp M

P

1

2

3

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM CHLA.PSI Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : CHLA.PSI Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CHLA.PSI Molecular Diagnostic

Catalog No. HUM0022(S)

HumPCRTM CHLA.PSI Detection Kit 48 or 96

HUM0022(48) HUM0022(96)

BrigTM Molecular Weight Marker

HUMAN

271 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CHLA.spp Detection Kit 2. SPECIMEN

Vaginal, urethral, or conjunctival swab. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Chlamydiae are obligate intracellular parasites of humans and animals. The different chlamydial species are very similar in the biology of their infection and developmental process. They exhibit a biphasic-life cycle with a smaller extracellular infectious form, the elementary body, and a larger replicating intracellular form, the reticulate body. Chlamydiae have a tropism for epithelial cells of the endocervix and upper genital tract of women, and the urethra, rectum and conjunctive of both sexes. As Chlamydiae need to pass an intracellular stage during their life cycle, they require tissue culture techniques to be isolated and propagated. Diagnosis by cell culture requires very experienced laboratory workers and standardized protocols. Non-culture test includes immunofluorescence, ELISA and PCR. HumPCR™ CHLA.SPP Detection Kit is the direct detection of Chlamydia spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 477bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM CHLA.spp Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : CHLA.spp Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CHLA.spp Molecular Diagnostic

Catalog No. HUM0023(S)

HumPCRTM CHLA.spp Detection Kit 48 or 96

HUM0023(48) HUM0023(96)

BrigTM Molecular Weight Marker

HUMAN

477 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CHLA.TRA Detection Kit 2. SPECIMEN

Urine (first void) or endocervical/urethral swab. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

HUMAN

Chlamydia trachomatis is a Gram-negative obligate intracellular bacterium with a biphasic development cycle in which they alternate between the infectious extracellular and metabolically inactive form (the elementary body) and the intracellular, metabollicaly active replicating form (the reticulate body). C. trachomatis infection is one of the most prevalent sexually transmitted infection and infectious disease in the world. Sexually active individuals and individuals with multiple partners are at highest risk. Chlamydia may be difficult to detect because early-stage infections often cause few or no signs and symptoms. If symptoms do occur, they usually appear within 1 to 3 weeks after exposure. Women who have symptoms might have an abnormal vaginal discharge or a burning sensation when urinating. When the infection spreads from the cervix to the fallopian tubes, some women have lower abdominal pain, low back pain, nausea, fever, pain during intercourse, or bleeding between menstrual periods. Men with signs or symptoms might have a discharge from their penis or a burning sensation when urinating. Men might also have burning and itching around the opening of the penis. Pain and swelling in the testicles are uncommon. C trachomatis is susceptible to antibiotics that interfere with protein or DNA synthesis, including macrolides, tetracyclines, quinolones, and sulfonamides. HumPCR™ CHLA.TRA Detection Kit is the direct detection of Chlamydia trachomatis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 256 bp M

1

2

3

P

N

300bp

256 bp

Fig1. Electrophoresis of PCR product by VetPCRTM CHLA.TRA Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : CHLA.TRA Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CHLA.TRA Molecular Diagnostic

Catalog No. HUM0023(S)

HumPCRTM CHLA.TRA Detection Kit 48 or 96

HUM0023(48) HUM0023(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CMV Detection Kit 2. SPECIMEN 1. DESCRIPTION

Whole blood, cerebrospinal fluid (CSF), serum, plasm, bone marrow or bronchoalveolar lavage. 3. INTERPRETATION OF RESULTS

Cytomegalovirus (CMV) or Human Herpes Virus 5, is a member of the Herpesviridae family. CMV is the most common congenital (present at birth) infection in the United States. This virus is found universally throughout all geographic locations and socioeconomic groups, and infects between 50% and 85% of adults in the United States by 40 years of age. CMV infection is more widespread in developing countries and in areas of lower socioeconomic conditions. For most healthy persons who acquire CMV after birth there are few symptoms. However, CMV infection is important to certain high-risk groups. Major areas of concern are: (1) the risk of infection to the unborn baby during pregnancy (2) the risk of infection to people who work with children (3) the risk of infection to the immunocompromised person, such as organ transplant recipients and persons infected with Human Immunodeficiency Virus (HIV) (4) the risk of infection to newborn babies. Lytically replicating virus disrupts the cytoskeleton, causing massive cell enlargement, which is the source of the virus’ name. HumPCRTM CMV Detection Kit is the direct detection of Cytomegalovirus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 488 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM CMV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : CMV Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CMV Molecular Diagnostic

Catalog No. HUM0025(S)

HumPCRTM CMV Detection Kit 48 or 96

HUM0025(48) HUM0025(96)

BrigTM Molecular Weight Marker

HUMAN

488 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM COX.BUR Detection Kit 2. SPECIMEN

Placental bits, genital swabs, fecal swabs, urine, whole blood. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Coxiella burnetii is a highly pleomorphic, Gram negative cocobacillus. The pleomorphic nature of the organism is due to the generation of morphologically distinct cell forms that arise as part of a bifasic developmental cycle. This organism is an obligate intracellular bacterium. C. burnetii has been identificated in arthropods, fish, birds, rodents, marsupials and livestock.

- Expected PCR product size : 406 bp M

1

2

3

P

N

406 bp

300bp

Q fever is a zoonosis caused by C. burnetii. Infection with C. burnetii can be acute or chronic, and exhibits a wide spectrum of clinical manifestations. The most common are pneumonia, hepatitis, and isolated fever. The main clinical manifestation of chronic Q fever is endocarditis. Primary infection in pregnant women, whether or not symptomatic, may be followed by abortion, prematurity, or low birth weight. The diagnosis of Q fever relies mainly on serologic examination. Several laboratory studies are available, but antibody detection by immunofluorescence assay is the most commonly used method because of its high sensitivity and specificity.

HUMAN

HumPCR™ COX.BUR Detection Kit is the direct detection of Coxiella burnetii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique..

Fig1. Electrophoresis of PCR product by VetPCRTM COX.BUR Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : COX.BUR Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM COX.BUR Molecular Diagnostic

Catalog No. HUM0026(S)

HumPCRTM COX.BUR Detection Kit 48 or 96

HUM0026(48) HUM0026(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM CRYPTO Detection Kit 2. SPECIMEN

Fecal samples. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Cryptosporidium are coccidian protozoan parasites which belong to the phylum Apicomplexa, class Sporozasida, subclass Coccidiasina. Many species of Crytosporidia have been identificated in most vertebrates. The ability to transmit infection between species, most notably between animals and man, indicates that this zoonotic organism lacks host specificity. The life cycle of most Cryptosporidium species is completed within the gastrointestinal tract of the host, with developmental stages being associated with the luminal surface of the mucosal epithelial cells. Cryptosporidiosis in humans is a disease with a median duration of 9–15 days, their major symptom is watery diarrhea associated with abdominal cramps, anorexia, weight loss, nausea, vomiting, fatigue and low-grade fever. In inmuno-comprimised patients, such as those with HIV, cryptosporidiosis can become a life-threatening condition causing profuse intractable diarrhea with severe dehydration, malabsorption and wasting. These symptoms can persist unabated until the patient eventually dies. HumPCR™ CRYPTO Detection Kit is the direct detection of Cryptosporidium on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 460 bp M

1

2

3

P

N

Fig1. Electrophoresis of PCR product by VetPCRTM CRYPTO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : CRYPTO Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM CRYPTO Molecular Diagnostic

Catalog No. HUM0027(S)

HumPCRTM CRYPTO Detection Kit 48 or 96

HUM0027(48) HUM0027(96)

BrigTM Molecular Weight Marker

HUMAN

460 bp

400bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM E.COLI O157:H7 Detection Kit 2. SPECIMEN 1. DESCRIPTION

Urine, stool, wound swabs, vaginal swabs, urethral swabs, endocervical swabs, ear swabs, semen, cerebrospinal fluid (CSF), whole blood. 3. INTERPRETATION OF RESULTS

Escherichia coli is a member of the normal intestinal flora. Strains of E. coli that produce verocytotoxin, such as E. coli O157:H7, form an important group of zoonotic pathogens of significant worldwide public health concern. E. coli O157:H7 has become an important cause of severe gastrointestinal illness, often causing bloody diarrhoea that can progress to more serious illness, including haemolytic uraemic syndrome and death. Transmission of E. coli O157:H7 to humans is principally via contamination of food by animal faeces, with cattle considered to be the primary reservoir. Several other species including rabbits, deer, water buffalo, pigs, chickens and seagulls have also been implicated as carriers of E. coli O157:H7. Rapid methods to detect E. coli O157:H7 are important for public health purposes, such as finding outbreaks. Culture-based methods for the detection of E. coli O157:H7 are slow and labor intensive. HumPCRTM E.COLI O157:H7 Detection Kit is the direct detection of Escherichia coli O157:H7 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 213 bp M

1

2

3

P

N

300bp 213 bp Fig1. Electrophoresis of PCR product by VetPCRTM E.COLI O157:H7 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : E.COLI O157:H7 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM E.COLI O157:H7 Molecular Diagnostic

Catalog No. HUM0028(S)

HumPCRTM E.COLI O157:H7 Detection Kit 48 or 96

HUM0028(48) HUM0028(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM EHRL.CAN Detection Kit 2. SPECIMEN

Whole blood, cerebrospinal fluid (CSF). 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Ehrlichia canis is a small obligate intracellular, Gram-negative, dimorphic bacterium. It resides as a microcolony inside an intracellular vacuole that is membrane-lined and is mainly within monocytes and macrophages of mammalian hosts. This organism is primarily transmitted by Rhipicephalus sanguineus, the brown dog tick. Human monocytic ehrlichiosis (HME) is caused by E. chaffeensis and E. canis. Clinical signs of HME vary from asymptomatic infection to severe illness which requires hospitalization, or even death. Severe HME is characterized by fever, chill, headache, myalgia, anorexia, nausea or vomiting, and weight loss. These clinical signs are similar to Rocky Mountain spotted fever, influenza, infectious mononucleosis, and dengue fever. Because diagnostic tests are not widely available, the diagnosis of ehrlichiosis is usually based on symptoms and a history of exposure to ticks. HumPCRTM EHRL.CAN Detection Kit is the direct detection of Ehrlichia canis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 238 bp M

N

P

1

2

3

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM EHRL.CAN Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~3 : EHRL.CAN Positive sample 4. ORDERING INFORMATION Product HumPCRTM EHRL.CAN Molecular Diagnostic

Catalog No. HUM0030(S)

HumPCRTM EHRL.CAN Detection Kit 48 or 96

HUM0030(48) HUM0030(96)

BrigTM Molecular Weight Marker

HUMAN

238 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM EHRL.CHA Detection Kit 2. SPECIMEN

Whole blood or bone marrow. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Ehrlichia chaffeensis are cocci, Gram-negative bacteria in the family Rickettsiaceae. This organism is an obligate intracellular parasite and show tropism for monocytes where resides as a microcolony in a membranelined intracellular vacuole (morula), causing human monocytic ehrlichiosis, a zoonotic disease transmitted to humans by ticks. White-tailed deer and dog are the main reservoirs. The clinical symptoms range in severity from minor confusion and lethargy, to meningismus, cranial nerve palsies, seizures, and coma. Long term sequelae of neurologic involvement are not common, but patients may take weeks to months to fully recover. Human ehrlichiosis can be diagnosed by collecting blood in EDTA or collecting cerebrospinal fluid and performing culture, histological analysis, nuclei acid amplification or serological detection of specific antibodies. HumPCR™ EHRL.CHA Detection Kit is the direct detection of Ehrlichia chaffeensis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 238 bp M

N

1

2

3

P

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM EHRL.CHA Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : EHRL.CHA Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM EHRL.CHA Molecular Diagnostic

Catalog No. HUM0031(S)

HumPCRTM EHRL.CHA Detection Kit 48 or 96

HUM0031(48) HUM0031(96)

BrigTM Molecular Weight Marker

HUMAN

238 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM EHRL.spp Detection Kit 2. SPECIMEN

Whole blood or bone marrow. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Ehrlichia species are tick-transmitted intracellular bacteria closely related to Anaplasma, Neorickettsia and Rickettsia. Ehrlichiosis can have serious effects on an otherwise healthy adult or child if you don’t seek prompt treatment. Ehrlichiosis causes flu-like symptoms. The signs and symptoms of ehrlichiosis range from mild body aches to severe fever and usually appear within a week or two of a tick bite. If treated quickly with antibiotics, ehrlichiosis generally improves within a few days. HumPCRTM EHR.spp Detection Kit is the direct detection of Ehrlichia spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 282 bp M

P

1

2

3

N

300bp

282 bp

Fig1. Electrophoresis of PCR product by VetPCRTM EHRL.spp Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : EHRL.spp Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM EHRL.spp Molecular Diagnostic

Catalog No. HUM0032(S)

HumPCRTM EHRL.spp Detection Kit 48 or 96

HUM0032(48) HUM0032(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM ENTERO.VRE Detection Kit 2. SPECIMEN 1. DESCRIPTION

Swab specimen of nares, axilla, torso, rectum, groin in bacterial transport; urine; stool. 3. INTERPRETATION OF RESULTS

Enterococci are bacteria that live in the human digestive tract and female genital tract and generally do not cause disease. Vancomycin-Resistant Enterococcus (VRE) is a mutant strain of Enterococcus that is resistant to the antibiotic vancomycin. Enterococci have two types of resistance to vancomycin: acquired and intrinsic (natural). Some strains of enterococci bacteria acquire the resistance when other bacteria come in contact with enterococci and share genetic information. VRE threatens to compromise effective treatment of infections caused by these multi-resistant gram-positive bacteria, particularly in seriously ill, hospitalized patients who may need treatment with vancomycin where other antibiotics have failed. Therapeutic alternatives for antibiotic treatment are still insufficient. Therefore, rapid typing of resistances that appear, as well as enterococci differentiation, is of major therapeutic and epidemiological significance. Conventional methods can only detect the phenotypical characteristics of the resistance and not, however, the genetic background. In addition, they are very time-consuming, with a reliable diagnosis being determined only after 2-5 days. HumPCRTM ENTERO.VRE Detection Kit is the direct detection of Vancomycin-Resistant Enterococcus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 278 bp M

P

1

2

3

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM ENTERO.VRE Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : ENTERO.VRE Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM ENTERO.VRE Molecular Diagnostic

Catalog No. HUM0033(S)

HumPCRTM ENTERO.VRE Detection Kit 48 or 96

HUM0033(48) HUM0033(96)

BrigTM Molecular Weight Marker

HUMAN

278 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM ENTERO.FAE Detection Kit 2. SPECIMEN 1. DESCRIPTION

Swab specimen of nares, axilla, torso, rectum, groin in bacterial transport; urine; stool. 3. INTERPRETATION OF RESULTS

Enterococcus faecalis is a nonmotile, gram-positive, spherical bacterium. It is a facultative anaerobe with a fermentative metabolism. E. faecalis are a part of the normal intestinal flora of both humans and animals. The bacterium is such a regular a component of the intestinal flora, that many European countries use it as the standard indicator of fecal pollution E. faecalis are the leading cause of nosocomial infection. They are a common cause of urinary tract and wound infections. They can disseminate from the gastrointestinal tract to cause cholangitis, peritonitis, and intraabdominal abscess, often as part of a polymicrobial infection. Bacteremia and endocarditis are other well-recognized clinical manifestations. Culture and identification of E. faecalis require 2 to 3 days to provide results. HumPCRTM ENTERO.FAE Detection Kit is the direct detection of Enterococcus faecalis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 256 bp M

N

P

1

2

3

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM ENTERO.FAE Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~3 : ENTERO.FAE Positive sample 4. ORDERING INFORMATION Product HumPCRTM ENTERO.FAE Molecular Diagnostic

Catalog No. HUM0034(S)

HumPCRTM ENTERO.FAE Detection Kit 48 or 96

HUM0034(48) HUM0034(96)

BrigTM Molecular Weight Marker

HUMAN

256 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM FRAN.TUL Detection Kit 2. SPECIMEN 1. DESCRIPTION

Sputum, bronchial wash or bronchoalveolar lavage (BAL), biopsy specimens of infected soft-tissue or lymph nodes. 3. INTERPRETATION OF RESULTS

Francisella tularensis is a nonmotile, aerobic, gram-negative cocobacillus. F. tularensis is a facultative intracellular bacterium and one of the most infectious pathogenic bacteria known; the infective dose may be as low as 10 organisms. Tularemia is a zoonotic infection caused by F. tularensis. The type and severity of the disease is dependent on strain, dose and route of infection. The incubation period is 3–5 days normally and patients develop flu-like symptoms. The most common form of the disease is ulceroglandular tularemia; ulcers may result from contact with contaminated animal products or from an arthropod vector. HumPCR™ FRAN.TUL Detection Kit is the direct detection of Francisella tularensis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 346 bp M

1

2

3

P

N

Fig1. Electrophoresis of PCR product by VetPCRTM FRAN.TUL Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : FRA.TUL Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM FRAN.TUL Molecular Diagnostic

Catalog No. HUM0035(S)

HumPCRTM FRAN.TUL Detection Kit 48 or 96

HUM0035(48) HUM0035(96)

BrigTM Molecular Weight Marker

HUMAN

346 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM FUS.SPP Detection Kit 2. SPECIMEN 1. DESCRIPTION

Pus, tissue, or other material properly obtained from an abscess, biopsy, aspirate, drainage, exudate, lesion, or wound. 3. INTERPRETATION OF RESULTS

The genus Fusobacterium includes several species of anaerobic, non-sporeforming, Gram negative rods. Fusobacterium species are found in the mucous membranes of humans and animals. There are about 20 species in the genus of which the most important clinically are F. nucleatum and F. necrophorum. F. nucleatum is commonly found in periodontal disease and produces tissue irritants such as butyric acid which contributes to halitosis. Butyrate inhibits proliferation of human gingival fibroblasts and may penetrate the gingival epithelium. Necrobacillosis is an infection caused by F. necrophorum. Lemierre’s syndrome is the classical presentation of human necrobacillosis. It is characterized by a primary infection in the head which subsequently develops with persistent high fever and disseminated metastatic abscesses, frequently including a septic thrombophlebitis of the internal jugular vein. HumPCR™ FUS.SPP Detection Kit is the direct detection of Fusobacterium spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 452 bp M

1

2

3

P

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM FUS.SPP Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : FUS.SPP Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM FUS.SPP Molecular Diagnostic

Catalog No. HUM0036(S)

HumPCRTM FUS.SPP Detection Kit 48 or 96

HUM0036(48) HUM0036(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM GAR.VAGI Detection Kit 2. SPECIMEN Vaginal swab samples, semen. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Gardnerella vaginalis cells are Gram-variable, small, pleomorphic rods that are nonmotile and do not possess flagella, endospores, or typical capsules. The physiological state of the bacteria affects their morphology and staining reactions. It is presents as normal vaginal flora in approximately 40% to 50% of normal healty woman. Bacterial vaginosis (BV) is characterized by a shift in the vaginal flora from the dominant flora of Lactobacillus spp. to a mixed vaginal flora that includes G. vaginalis, Bacterioides spp., Mobiluncus spp. and Mycoplasma hominis. An increase in vaginal discharge and vaginal malodor characterizes BV. In pregnancy, BV can cause premature labor, premature birth, infection of the amniotic fluid, and infection of the uterus after delivery. Diagnosis of BV is complicated by the polymicrobial nature of the condition. The Gram stain is a common method for diagnosing bacterial vaginosis. HumPCR™ GAR.VAGI Detection Kit is the direct detection of Gardnerella vaginalis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 331bp M

P

1

2

3

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM GAR.VAGI Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : GAR.VAGI Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM GAR.VAGI Molecular Diagnostic

Catalog No. HUM0037(S)

HumPCRTM GAR.VAGI Detection Kit 48 or 96

HUM0037(48) HUM0037(96)

BrigTM Molecular Weight Marker

HUMAN

331 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM GAR.VAGI-TR Detection Kit 2. SPECIMEN

0.5 ml whole blood in EDTA (purple top) tube. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Gardnerella vaginalis is a pleomorphic, Gram-variable coccobacilli. This bacteria has been associated with Bacterial Vaginosis (BV), a polymicrobial superficial vaginal infection involving a loss of the normal lactobacilli and an overgrowth of anaerobes. Besides being implicated in BV, G. vaginalis has been associated with conditions such as chorioamnionitis, urinary tract infections, bacteremia in adults and neonatal meningitis Treatment for BV consists of antibiotics. Tetracycline is an antibiotic that has a broad spectrum of activity and low toxicity. Tetracyclines are the second most commonly used antibiotic type worldwide; however, their efficacy has been reduced by the increase in microbial resistance to the drug. High-level tetracycline resistant in strains of G. vaginalis examined to date has the Tet M determinant, encoding resistance to tetracycline, on the chromosome. HumPCR™ GAR.VAGI-TR Detection Kit is the direct detection of Gardnerella vaginalis tetracycline resistant on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 452 bp M

P

1

2

3

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM GAR.VAGI-TR Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : GAR.VAGI-TR Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM GAR.VAGI-TR Molecular Diagnostic

Catalog No. HUM0038(S)

HumPCRTM GAR.VAGI-TR Detection Kit 48 or 96

HUM0038(48) HUM0038(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM GIAR.LAM Detection Kit 2. SPECIMEN Fecal samples. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Giardia, a genus of primitive eukaryotes, is a flagellated enteric protozoan of the class Zoomastigophorea. The G. lamblia cycle has two stages, the cyst, which transmits disease to the host, and the trophozoite, which causes disease. Unlike other protozoans parasites, G. lamblia is a extracellular protozoan. The G. lamblia is the most prevalent parasite in the world. Transmission has been associated with contaminated water and person-to-person spread. Most outbreaks are related to untreated or inadequately purified water. Person-to-person transmission is related to poor fecal-oral hygiene. Giardiasis is rather difficult to diagnose, in part because the organism is difficult to detect. Testing for G. lamblia requires the search for individual, organism under a microscope. HumPCR™ GIAR.LAM Detection Kit is the direct detection of Giardia lamblia on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 415 bp M

N

P

1

2

3

4

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM GIAR.LAM Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~4 : GIAR.LAM Positive sample 4. ORDERING INFORMATION Product HumPCRTM GIAR.LAM Molecular Diagnostic

Catalog No. HUM0039(S)

HumPCRTM GIAR.LAM Detection Kit 48 or 96

HUM0039(48) HUM0039(96)

BrigTM Molecular Weight Marker

HUMAN

415 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HAM.INFLU Detection Kit 2. SPECIMEN

Nasopharyngeal swabs, pus, whole blood, cerebrospinal fluid (CSF). 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Haemophilus influenzae is a small, pleomorphic, Gram-negative coccobacillus. It is a nonmotile, nonspore-forming, facultative anaerobe. There are six serotypes of H. influenzae (a to f ) based on their biochemically different capsules, of which the most virulent is Haemophilus influenzae type b (Hib). The carrier rate in the upper respiratory tract for Hib is 2-4%. The carrier rate for nontypeable H. influenzae is 50-80%. Infection with Hib can result in meningitis and other infections like pneumonia, epiglottitis, septic arthritis, cellulitis, and bacteremia, primarily among infants and children. Hib disease is uncommon in individuals 5 years of age or older. Hib may be transmitted through contact with mucus or droplets from the nose and throat of an infected person. HumPCR™ HAM.INFLU Detection Kit is the direct detection of Haemophilus influenzae on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 254 bp M

1

2

3

P

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM HAM.INFLU Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HAM.INFLU Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HAM.INFLU Molecular Diagnostic

Catalog No. HUM0040(S)

HumPCRTM HAM.INFLU Detection Kit 48 or 96

HUM0040(48) HUM0040(96)

BrigTM Molecular Weight Marker

HUMAN

254 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HELI.PYL Detection Kit 2. SPECIMEN

0.5 ml whole blood in EDTA (purple top) tube. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Helicobacter pylori is a gram-negative, spiral-shaped bacterium. H. pylori infection is the most common cause of stomach ulcers, and it also causes inflammation of the stomach lining. H. pylori infection may also contribute to stomach cancers and other digestive system cancers. H. pylori infection may be present in about half the people in the world. In industrialized countries the infection rate is about 20 percent to 30 percent, but in developing countries the infection rate may exceed 70 percent. However, most people who carry the bacteria experience no signs or symptoms of infection. HumPCRTM HELI.PYL Detection Kit is the direct detection of Helicobacter pylori on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique

- Expected PCR product size : 546 bp M

N

P

1

2

3

4

500bp

546 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HELI.PYL Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~4 : HELI.PYL Positive sample 4. ORDERING INFORMATION Product HumPCRTM HELI.PYL Molecular Diagnostic

Catalog No. HUM0041(S)

HumPCRTM HELI.PYL Detection Kit 48 or 96

HUM0041(48) HUM0041(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HHV-6 Detection Kit 2. SPECIMEN 1. DESCRIPTION

Human herpesvirus 6 (HHV-6) belongs to the Roseolavirus genus of the Ă&#x;-herpesvirus subfamily and was discovered in 1986. HHV-6 is ubiquitous in general populations, with up to 90% of the adults being seropositive. Human Herpes Virus 6 consists of two closely related yet distinct viruses, designated human Herpes Virus 6 variant A (HHV-6A) and Human Herpes Virus 6 variant B (HHV-6B). The most frequent manifestation of acute primary HHV-6 infection is roseola infantum in babies and young children. HHV-6 reactivation has been shown to play a role in the pathogenesis of AIDS and several other diseases. Assays for HHV-6 antibodies are most useful in young children who are undergoing primary infection. In these children seroconversion is diagnostic of acute infection.

HUMAN

HumPCR™ HHV-6 Detection Kit is the direct detection of Human herpesvirus 6 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Whole blood, plasma, bone marrow, bronchial wash or bronchoalveolar lavage (BAL), cerebrospinal fluid (CSF). 3. INTERPRETATION OF RESULTS - Expected PCR product size : 415 bp M

N

1

2

3

P

415 bp

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM HHV-6 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HHV-6 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HHV-6 Molecular Diagnostic

Catalog No. HUM0042(S)

HumPCRTM HHV-6 Detection Kit 48 or 96

HUM0042(48) HUM0042(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HHV-8 Detection Kit 2. SPECIMEN 1. DESCRIPTION

Human herpesvirus 8 (HHV-8) is a member of Rhadinovirus and possesses a typical herpesvirus morphology with a central icosahedral capsid surrounded by a lipid bilayer. HHV-8 contributes to the development of Kaposi sarcoma and two other lymphoproliferative disorders in the AIDS setting: primary effusion lymphoma and the plasma cell variant of multicentric Castleman’s disease. HHV-8 persists in a latent form for life, with CD19+ B cells as the main reservoir. HHV-8 infection occurs at low levels among children in nonendemic areas. However, in countries where the virus is endemic, seroprevalence may reach adult levels before adolescence, suggesting that transmission among children may occur through close, nonsexual contact. Sexual transmission is thought to be the main route of infection in male homosexuals.

HUMAN

HumPCR™ HHV-8 Detection Kit is the direct detection of Human herpesvirus 8 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Whole blood, plasma, bone marrow, bronchial wash or bronchoalveolar lavage (BAL), cerebrospinal fluid (CSF). 3. INTERPRETATION OF RESULTS - Expected PCR product size : 406 bp M

1

2

3

P

N

400bp

406 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HHV-8 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HHV-8 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HHV-8 Molecular Diagnostic

Catalog No. HUM0043(S)

HumPCRTM HHV-8 Detection Kit 48 or 96

HUM0043(48) HUM0043(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV Detection Kit 2. SPECIMEN 1. DESCRIPTION

Pus, tissue, or other material properly obtained from an abscess, biopsy, aspirate, drainage, exudate, lesion, or wound. 3. INTERPRETATION OF RESULTS

The genus Fusobacterium includes several species of anaerobic, non-sporeforming, Gram negative rods. Fusobacterium species are found in the mucous membranes of humans and animals. There are about 20 species in the genus of which the most important clinically are F. nucleatum and F. necrophorum. F. nucleatum is commonly found in periodontal disease and produces tissue irritants such as butyric acid which contributes to halitosis. Butyrate inhibits proliferation of human gingival fibroblasts and may penetrate the gingival epithelium. Necrobacillosis is an infection caused by F. necrophorum. Lemierre’s syndrome is the classical presentation of human necrobacillosis. It is characterized by a primary infection in the head which subsequently develops with persistent high fever and disseminated metastatic abscesses, frequently including a septic thrombophlebitis of the internal jugular vein. HumPCR™ FUS.SPP Detection Kit is the direct detection of Fusobacterium spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 452 bp M

1

2

3

P

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM FUS.SPP Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : FUS.SPP Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM FUS.SPP Molecular Diagnostic

Catalog No. HUM0036(S)

HumPCRTM FUS.SPP Detection Kit 48 or 96

HUM0036(48) HUM0036(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-11 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract. Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues. Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. Types 6 and 11 – which are linked to about 90 percent of genital warts – are the most common.

HUMAN

HumPCR™ HPV-11 Detection Kit is the direct detection of Human papillomavirus type 11 (HPV type 11) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 439 bp M

N

1

2

3

P

400bp

439 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-11 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-11 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-11 Molecular Diagnostic

Catalog No. HUM0045(S)

HumPCRTM HPV-11 Detection Kit 48 or 96

HUM0045(48) HUM0045(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-16 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-16 Detection Kit is the direct detection of Human papillomavirus type 16 (HPV type 16) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 299 bp M

1

2

3

P

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-16 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HPV-16 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-16 Molecular Diagnostic

Catalog No. HUM0046(S)

HumPCRTM HPV-16 Detection Kit 48 or 96

HUM0046(48) HUM0046(96)

BrigTM Molecular Weight Marker

HUMAN

299 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-18 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-18 Detection Kit is the direct detection of Human papillomavirus type 18 (HPV type 18) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 346 bp M

N

1

2

3

P

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-18 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-18 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-18 Molecular Diagnostic

Catalog No. HUM0047(S)

HumPCRTM HPV-18 Detection Kit 48 or 96

HUM0047(48) HUM0047(96)

BrigTM Molecular Weight Marker

HUMAN

346 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-30 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-30 Detection Kit is the direct detection of Human papillomavirus type 30 (HPV type 30) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 366 bp M

1

2

3

P

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-30 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HPV-30 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-30 Molecular Diagnostic

Catalog No. HUM0048(S)

HumPCRTM HPV-30 Detection Kit 48 or 96

HUM0048(48) HUM0048(96)

BrigTM Molecular Weight Marker

HUMAN

366 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-31 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-31 Detection Kit is the direct detection of Human papillomavirus type 31 (HPV type 31) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 187 bp M

N

1

2

3

P

200bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-31 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-31 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-31 Molecular Diagnostic

Catalog No. HUM0049(S)

HumPCRTM HPV-31 Detection Kit 48 or 96

HUM0049(48) HUM0049(96)

BrigTM Molecular Weight Marker

HUMAN

187 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-33 Detection Kit 2. SPECIMEN 1. DESCRIPTION

Cervical swab, cervical biopsy. 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-33 Detection Kit is the direct detection of Human papillomavirus type 33 (HPV type 33) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 366 bp M

N

1

2

3

P

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-33 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-33 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-33 Molecular Diagnostic

Catalog No. HUM0050(S)

HumPCRTM HPV-33 Detection Kit 48 or 96

HUM0050(48) HUM0050(96)

BrigTM Molecular Weight Marker

HUMAN

366 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-35 Detection Kit 2. SPECIMEN 1. DESCRIPTION

Cervical swab, cervical biopsy. 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-35 Detection Kit is the direct detection of Human papillomavirus type 35 (HPV type 35) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 284 bp M

N

1

2

3

P

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-35 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-35 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-35 Molecular Diagnostic

Catalog No. HUM0051(S)

HumPCRTM HPV-35 Detection Kit 48 or 96

HUM0051(48) HUM0051(96)

BrigTM Molecular Weight Marker

HUMAN

284 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-40 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract. Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues. Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. HumPCR™ HPV-40 Detection Kit is the direct detection of Human papillomavirus type 40 (HPV type 40) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 374 bp M

P

1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-40 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : HPV-40 Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-40 Molecular Diagnostic

Catalog No. HUM0052(S)

HumPCRTM HPV-40 Detection Kit 48 or 96

HUM0052(48) HUM0052(96)

BrigTM Molecular Weight Marker

HUMAN

374 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-42 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract. Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues. Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. HumPCR™ HPV-40 Detection Kit is the direct detection of Human papillomavirus type 40 (HPV type 40) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 374 bp M

P

1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-40 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : HPV-40 Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-40 Molecular Diagnostic

Catalog No. HUM0052(S)

HumPCRTM HPV-40 Detection Kit 48 or 96

HUM0052(48) HUM0052(96)

BrigTM Molecular Weight Marker

HUMAN

374 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-43 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract. Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues. Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. HumPCR™ HPV-43 Detection Kit is the direct detection of Human papillomavirus type 43 (HPV type 43) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 394 bp M

P

1

2

3

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-43 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : HPV-43 Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-43 Molecular Diagnostic

Catalog No. HUM0054(S)

HumPCRTM HPV-43 Detection Kit 48 or 96

HUM0054(48) HUM0054(96)

BrigTM Molecular Weight Marker

HUMAN

394 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-44 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract. Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues. Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. HumPCR™ HPV-44 Detection Kit is the direct detection of Human papillomavirus type 44 (HPV type 44) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 254 bp M

N

1

2

3

P

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-44 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-44 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-44 Molecular Diagnostic

Catalog No. HUM0055(S)

HumPCRTM HPV-44 Detection Kit 48 or 96

HUM0055(48) HUM0055(96)

BrigTM Molecular Weight Marker

HUMAN

254 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-45 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection (types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-45 Detection Kit is the direct detection of Human papillomavirus type 45 (HPV type 45) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 483 bp M

N

1

2

3

4

P

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-45 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~4 : HPV-45 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-45 Molecular Diagnostic

Catalog No. HUM0056(S)

HumPCRTM HPV-45 Detection Kit 48 or 96

HUM0056(48) HUM0056(96)

BrigTM Molecular Weight Marker

HUMAN

483 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-51 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection ((types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-51 Detection Kit is the direct detection of Human papillomavirus type 51 (HPV type 51) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 664 bp M

1

2

3

P

N

700bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-51 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HPV-51 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HPV-51 Molecular Diagnostic

Catalog No. HUM0057(S)

HumPCRTM HPV-51 Detection Kit 48 or 96

HUM0057(48) HUM0057(96)

BrigTM Molecular Weight Marker

HUMAN

664 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-52 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection ((types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-52 Detection Kit is the direct detection of Human papillomavirus type 52 (HPV type 52) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 386 bp M

N

1

2

3

P

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-52 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : HPV-52 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-52 Molecular Diagnostic

Catalog No. HUM0058(S)

HumPCRTM HPV-52 Detection Kit 48 or 96

HUM0058(48) HUM0058(96)

BrigTM Molecular Weight Marker

HUMAN

386 bp

300bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-56 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Human papillomaviruses (HPV) are a group of DNA virus. More than 100 genotypes have been identified, causing benign (low-risk HPV) or malignant (high-risk HPV) cutaneous or mucosal lesions. High-risk human papillomavirus (HR-HPV) is recognized as the primary cause for the development of cervical cancers and their precursor lesions. Clinical and epidemiological studies have confirmed that high-risk human papillomavirus (HR-HPV) infection ((types 16, 18, 30, 31, 33, 35, 45, 51, 52, 56, 58, 59) is the direct cause of cervical intraepithelial neoplasia (CIN) and cancers. High-risk HPV infection, is very common in young sexually active women. High-risk HPV are transmitted through sexual contact with an infected person. Condoms do not completely prevent HPV transmission, although consistent condom use has been demonstrated to reduce the risk of acquiring HPV by 70%. HumPCR™ HPV-56 Detection Kit is the direct detection of Human papillomavirus type 56 (HPV type 56) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 419 bp M

N

1

2

3

4

P

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-56 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~4 : HPV-56 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HPV-56 Molecular Diagnostic

Catalog No. HUM0059(S)

HumPCRTM HPV-56 Detection Kit 48 or 96

HUM0059(48) HUM0059(96)

BrigTM Molecular Weight Marker

HUMAN

419 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HPV-6 Detection Kit 2. SPECIMEN

Cervical swab, cervical biopsy. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

HUMAN

Human papillomaviruses (HPV) are a group of double stranded DNA viruses which infect the squamous epithelia of the skin or the mucous membranes. More than 100 genotypes have been identified, which have been categorized as being of low or high oncogenic risk based on their association with benign epithelial proliferations, high-grade cancer precursors, or invasive carcinomas of the anogenital tract.

- Expected PCR product size : 219 bp M

N

P

1

2

3

4

219 bp

200bp

Infection with HPV is basically a sexually transmitted disease. Both men and women are involved in the epidemiological chain of infection and are able at the same time to be asymptomatic carriers, transmitters and also victims of the infection by HPV. Because HPV do not grown in culture, HPV infection is most accurately measured by detection of specific DNA sequences in tissues.

Fig1. Electrophoresis of PCR product by VetPCRTM HPV-6 Detection Kit

Low-risk HPV (include HPV types 6, 11, 40, 42, 43, 44) are associated with benign genital warts. These lesions are fleshy, non-vascular warts that appear in the genital area and anal region of both men and women. They are caused by proliferation of the keratinized epithelium and may occur anywhere on the external genitalia. Types 6 and 11 – which are linked to about 90 percent of genital warts – are the most common.

4. ORDERING INFORMATION

HumPCR™ HPV-6 Detection Kit is the direct detection of Human papillomavirus type 6 (HPV type 6) on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique

Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~4 : HPV-6 Positive sample

Product HumPCRTM HPV-6 Molecular Diagnostic

Catalog No. HUM0062(S)

HumPCRTM HPV-6 Detection Kit 48 or 96

HUM0062(48) HUM0062(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HSV-1 Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), swab, whole blood, serum, or plasma. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

All herpes viruses are structurally similar with an icosahedral core surrounded by a lipoprotein envelope and a genome composed of linear doublestranded DNA. The HSV-1 is the most common herpes simplex virus and most people develop it in childhood. By adulthood, up to 90% of people will have antibodies to HSV-1. Most primary infections are acquired through direct contact with a lesion or with infected body fluids (saliva, genital fluids, and exudates of active lesions). It is usually associated with infections of the lips, mouth, and face. HSV-1 causes gingivostomatitis, keratoconjunctivitis, encephalitis, herpes labialis, herpetic whitlow among others. HSV-1 is becoming the predominant cause of the first episode of genital herpes in young persons.

HUMAN

HumPCR™ HSV-1 Detection Kit is the direct detection of Herpes Simplex Virus type 1 virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 262 bp M

N

1

2

3

4

P

300bp

262 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HSV-1 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~4 : HSV-1 Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HSV-1 Molecular Diagnostic

Catalog No. HUM0063(S)

HumPCRTM HSV-1 Detection Kit 48 or 96

HUM0063(48) HUM0063(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HSV-2 Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), swab, whole blood, serum, or plasma. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

The HSVs are part of a large family of DNA viruses, of which eight are known to be infectious in humans. Herpes simplex virus type 2 (HSV-2) is the primary cause of genital herpes, a common sexually transmitted disease. Following primary infection at skin or mucosal surfaces, viral DNA is rapidly transported to the innervating ganglia by retrograde axonal transport. Here the viral genome circularizes and establishes a life-long latency in sensory neurons. Stress stimuli trigger the resumption of virus gene transcription and replication, resulting in clinically overt skin and mucosal lesions and/or asymptomatic shedding. Genital herpes is acquired by sexual contact, including orogenital contact, with contaminated secretions or mucosal surfaces. The clinical manifestation of genital herpes is influenced by viral type, host factors (including immunological competence and the presence of antibodies to the heterologous herpes virus simplex), and previous outbreaks.

HUMAN

HumPCR™ HSV-2 Detection Kit is the direct detection of Herpes Simplex Virus type 2 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 382 bp M

1

2

3

P

N

500bp 382 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HSV-2 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HSV-2 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HSV-2 Molecular Diagnostic

Catalog No. HUM0064(S)

HumPCRTM HSV-2 Detection Kit 48 or 96

HUM0064(48) HUM0064(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTMJCV Detection Kit 2. SPECIMEN

Plasma or serum. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

JC virus (JCV) is a human polyomavirus of the Polyomaviridae family, which also includes BK virus and simian vacuolating virus 40 (SV40). The human polyomaviruses, as with all polyomaviruses, are composed of small, nonenveloped, icosahedral virions with a supercoiled double-stranded DNA genome. JCV is ubiquitous in the human population, infecting children asymptomatically, then persisting in the kidney. The main mode of transmission of JCV is from parents to children through long-term cohabitation. JCV has been established as the causative agent in progressive multifocal leukoencephalopathy, a fatal demyelinating disease of the central nervous system that occurs mainly in immunosuppressed patients. Given the ubiquitous nature of the virus and its strong association with cancer in animal models, it is hypothesized that JCV plays a role in human cancers. HumPCRTM JCV Detection Kit is the direct detection of Polyomavirus JC on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 329 bp M

P

1

2

3

N

400bp

Fig1. Electrophoresis of PCR product by VetPCRTM JCV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : JCV Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM JCV Molecular Diagnostic

Catalog No. HUM0065(S)

HumPCRTM JCV Detection Kit 48 or 96

HUM0065(48) HUM0065(96)

BrigTM Molecular Weight Marker

HUMAN

329 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTMLEG.PNEU Detection Kit 2. SPECIMEN

Respiratory secretions, urine and serum. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Legionella pneumophila, the causative agent of the pneumonia-like Legionnaires’ disease, is an aerobic, small, Gram-negative bacilli. The clinical features of Legionnaires’ disease are usually not reliably distinguished from those reported in other bacterial pneumonias. The severity of symptoms ranges from mild respiratory illness to a fulminating course. Although legionellosis may behave as a multisystemic disease, fever and nonspecific respiratory manifestations are usually predominant. Progressive respiratory failure is the most common cause of death in legionellosis. Water is the natural habitat of Legionella, where they can resist, although usually in low concentration, the usual chlorine concentrations found in water distribution systems. Although the bacteria primarily spread through aerosolized water droplets, the infection can be transmitted in other ways, like aspiration and the soil. Legionnaires’ disease can be very serious and can cause death in up to 5% to 30% of cases.Can be treated with antibiotics, like quinolones (ciprofloxacin, levofloxacin, moxifloxacin, or gatifloxacin) and macrolides (azithromycin, clarithromycin, or erythromycin). HumPCR™ LEG.PNEU Detection Kit is the direct detection of Legionella pneumophila on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique..

- Expected PCR product size : 469 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM LEG.PNEU Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : LEG.PNEU Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM LEG.PNEU Molecular Diagnostic

Catalog No. HUM0066(S)

HumPCRTM LEG.PNEU Detection Kit 48 or 96

HUM0066(48) HUM0066(96)

BrigTM Molecular Weight Marker

HUMAN

469 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM LEIS.SPP Detection Kit 2. SPECIMEN

Bone marrow, spleen, liver, lymph nodes. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Leishmania are protozoa belonging to the order Kinetoplastida and the family Tripanosomatidae, characterized by two morphologic stages in their life cycle: amastigote, found intracellularly in vertebrates, and promastigote, found in the digestive tract of invertebrate hosts. Some species of Leishmania, which has worldwide distribution, are known to be pathogenic in humans. Leishmaniasis occurs as a spectrum of clinical syndromes, which are usually divided into cutaneous, mucocutaneous and visceral leishmaniasis. The epidemiology and clinical features of the disease are highly variable due to the interplay of numerous factors in the parasites, vectors, hosts and environments involved. HumPCR™ LEIS.SPP Detection Kit is the direct detection of Leishmania spp. on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 495 bp M

N

P

1

2

3

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM LEIS.SPP Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~3 : LEIS.SPP Positive sample 4. ORDERING INFORMATION Product HumPCRTM LEIS.SPP Molecular Diagnostic

Catalog No. HUM0067(S)

HumPCRTM LEIS.SPP Detection Kit 48 or 96

HUM0067(48) HUM0067(96)

BrigTM Molecular Weight Marker

HUMAN

495 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM LEP.INTER Detection Kit 2. SPECIMEN

Whole blood, cerebrospinal fluid (CSF), urine. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Leptospira interrogans is a slender, tightly coiled, Gram negative spirochete. Morphologilcally L. interrogans is indistisguishable from other leptospires. This bacteria inhabits the tubules of mammalians kidneys, specillay rodents, and are shed in urine. Leptospirosis is a zoonosis occurring as large outbreaks throughout the world caused by L. interrogans. Most leptospiral infections are either subclinical or self limiting. If left untrated more serious forms of the illness can result in spontaneous abortion, uveitis, jaundice, and damage of the liver, heart and kidney. Most infections are associated with rats, cattle, pigs or dogs. HumPCR™ LEP.INTER Detection Kit is the direct detection of Leptospira interrogans on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 452 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM LEP.INTER Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : LEP.INTER Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM LEP.INTER Molecular Diagnostic

Catalog No. HUM0068(S)

HumPCRTM LEG.INTER Detection Kit 48 or 96

HUM0068(48) HUM0068(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM LEP.spp Detection Kit 2. SPECIMEN

Whole blood, urine. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

The genus Leptospira belongs to the phylum Spirochaetes and comprises saprophytic and pathogenic species. This bacterium is a flexible, spiralshaped, Gram-negative spirochete with internal flagella. Leptospira can occupy diverse environments, habitats and life cycles. Leptospirosis affects both humans and animals, causing a wide range of symptoms in both. In humans, typical symptoms can include fever, headaches, chills, sore muscles, vomiting, jaundice, red eyes, abdominal pain, diarrhea, or rashes. Leptospirosis can become considerably dangerous if not treated, potentially leading to kidney damage, meningitis, liver failure, and respiratory problems. Leptospirosis is typically contracted by humans through water, food, or urine contact with an infected animal. Diagnosis of leptospirosis is usually based on serology. Antibodies may be detected in the blood within 5–7 days of symptom onset. Culture or demonstration of the organism under darkfield microscopy are both relatively insensitive. HumPCRTM LEP.SPP Detection Kit is the direct detection of Leptospira spp on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 348 bp M

P

1

2

3

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM LEP.SPP Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : LEP.SPP Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM LEP.SPP Molecular Diagnostic

Catalog No. HUM0069(S)

HumPCRTM LEG.SPP Detection Kit 48 or 96

HUM0069(48) HUM0069(96)

BrigTM Molecular Weight Marker

HUMAN

348 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM LIS.MONO Detection Kit 2. SPECIMEN

CSF, whole blood. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Listeria monocytogenes is a motile, non–spore-forming, gram-positive bacillus that has aerobic and facultatively anaerobic characteristics. Although is an uncommon cause of illness in the general population, is an important pathogen in pregnant patients, neonates, elderly individuals, and immunocompromised individuals. The incidence of listeriosis varies between 0.1 and 11.3/1,000,000 in different countries. The overall mortality rate of listeriosis is 20-30%. Of all pregnancy-related cases, 22% resulted in fetal loss or neonatal death, but mothers usually survive. The symptoms include fever, muscle aches, and sometimes gastrointestinal symptoms such as nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache, stiff neck, confusion, loss of balance, or convulsions can occur. L. monocytogenes are naturally susceptible to penicillins, aminoglycosides, trimethoprim, tetracycline, macrolides, and vancomycin. HumPCR™ LIS.MONO Detection Kit is the direct detection of Listeria monocytogenes on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 596 bp M

N

1

2

3

P

600bp 596 bp

Fig1. Electrophoresis of PCR product by VetPCRTM LIS.MONO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : LIS.MONO Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM LIS.MONO Molecular Diagnostic

Catalog No. HUM0070(S)

HumPCRTM LIS.MONO Detection Kit 48 or 96

HUM0070(48) HUM0070(96)

HUMAN

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM MRSA Detection Kit 2. SPECIMEN 1. DESCRIPTION

Staphylococcus aureus is a nonmotile, non–spore-forming, catalase-and coagulase positive Gram positive coccus. S. aureus is a common member of the human microflora of the skin and mucous membranes. This organism causes disease through their ability to spread widely in tissues causing boils, septicaemia, endocarditis, pneumonia or osteomyelitis. S. aureus also is responsible for toxin-mediated diseases, such as toxic shock syndrome, staphylococcal scalded-skin syndrome and staphylococcal food poisoning. Methicillin resistant Staphylococcus aureus (MRSA) is a type of Staphylococcus aureus that is resistant to the antibacterial activity of methicillin and other related antibiotics of the penicillin class. Compared with Methicillin-sensitive S. aureus, MRSA infections are associated with worse outcomes, including longer hospital stays and higher mortality rates.

HUMAN

HumPCR™ MRSA Detection Kit is the direct detection of Methicillin-resistant Staphylococcus aureus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Swab specimen of nares, axilla, torso, and groin. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 322 bp M

P

1

2

3

N

300bp

322 bp

Fig1. Electrophoresis of PCR product by VetPCRTM MRSA Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : MRSA Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM MRSA Molecular Diagnostic

Catalog No. HUM0071(S)

HumPCRTM MRSA Detection Kit 48 or 96

HUM0071(48) HUM0071(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM NEIS.GONO Detection Kit 2. SPECIMEN

Endocervical swab, urethral swab, (Rectal or pharyngeal swab). 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Neisseria gonorrhoeae responsible for the sexually transmitted disease gonorrhoea is an aerobic, Gram-negative diplococcus, transmission of which is almost always by sexual contact. Urethral and endocervical infections are most common, but infection also occurs in the pharynx or rectum after oral or anal intercourse. The first gonorrhea symptoms generally appear within two to 10 days after exposure to the bacterium. However, some people may be infected for months before signs or symptoms occur. In men, first there’s often a tingling sensation in the urethra. Later, urination becomes painful and you may notice a discharge from your penis. As the infection progresses, urethral pain usually becomes more pronounced and the discharge becomes more profuse and thick. In women, the signs and symptoms, if any, may be so mild you may not realize you have the infection. Often, the only clue that you may have gonorrhea comes when someone who you’ve had sexual contact with develops the disease. The infection usually affects the cervix and other reproductive organs as well as the urethra. HumPCRTM NEIS.GONO Detection Kit is the direct detection of Neisseria gonorrhoeae on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 506 bp M

1

2

3

P

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM NEIS.GONO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : NEIS.GONO Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM NEIS.GONO Molecular Diagnostic

Catalog No. HUM0079(S)

HumPCRTM NEIS.GONO Detection Kit 48 or 96

HUM0079(48) HUM0079(96)

BrigTM Molecular Weight Marker

HUMAN

506 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM PENCYS.JIRO Detection Kit 2. SPECIMEN

Bronchoalveolar lavage (BAL), sputum. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Pneumocystis is a genus of unicellular fungi found in the respiratory tracts of many mammals and humans. The organism is found in 3 distinct morphologic stages, the trophozoite (trophic form), the sporozoite (precystic form) and the cyst, which contains several intracystic bodies (spores). Pneumocystis pneumonia, which is caused by Pneumocystis jirovecii (formerly P. carinii f. sp. hominis), is frequently the first serious illness encountered by HIV-infected persons. Patients in the developing world without access to PCP prophylaxis or antiretroviral drugs remain at high risk, and PCP continues to develop in certain groups in industrialized countries. Since P. jirovecii cannot be cultured, specific identification depends on examining respiratory specimens. These might include expectorated sputum and bronchoscopy with bronchoalveolar lavage. Laboratory identification of PCP is accomplished by microscopic examination using a variety of stains, such as Gomori methenamine silver or Wright-Giemsa. HumPCR™ PENCYS.JIRO Detection Kit is the direct detection of Pneumocystis jirovecii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 607 bp M

P

1

2

3

N

600bp

Fig1. Electrophoresis of PCR product by VetPCRTM PENCYS.JIRO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : PENCYS.JIRO Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM PENCYS.JIRO Molecular Diagnostic

Catalog No. HUM0080(S)

HumPCRTM PENCYS.JIRO Detection Kit 48 or 96

HUM0080(48) HUM0080(96)

BrigTM Molecular Weight Marker

HUMAN

607 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM PARV.B19 Detection Kit 2. SPECIMEN

Whole blood, serum, plasma, bone marrow, or cerebrospinal fluid (CSF). 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Parvovirus B-19 is a linear, nonenveloped, encapsulated, icosahedral, single-stranded DNA virus with a terminal hairpin structure that forms a double-stranded section characteristic of the Parvoviridae family. Parvovirus B-19 is the only parvovirus that is known to cause disease in humans. Human parvovirus B-19 is a common infection worldwide with a wide spectrum of clinical manifestations including erythremia infectiosum, arthralgia, arthritis, and transient aplastic anemia in immunocompetent individuals. However, it can evolve into a chronic, persistent infection in immunocompromised patients. Parvovirus B-19 is the cause of several distinct clinical syndromes including upper respiratory infection symptoms, polyarthralgia, and aplastic crisis, particularly in primary school-aged children. HumPCRTM PARV.B19 Detection Kit is the direct detection of Parvovirus B-19 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 531 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM PARV.B19 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : PARV.B19 Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM PARV.B19 Molecular Diagnostic HumPCRTM PARV.B19 Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

531 bp

Catalog No. HUM0081(S) HUM0081(48) HUM00781(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM STRE.AGAL Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), whole blood, vaginal swab. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

HUMAN

Streptococcus agalactiae is one of four Beta-Hemolytic streptococci, associated with complete lysis of red cells surrounding the colony on blood agar. S. agalactiae is a diplococcal, Gram-positive, non-motile, catalase negative bacterium. It is found normally in the gastrointestinal and genitourinary tract.

- Expected PCR product size : 713 bp M

1

2

3

P

N

700bp

713 bp

S. agalactiae is one of the major causes of meningitis and septicemia among newborns. They become infected during delivery through maternal genital tracts colonized with the bacterium. Adult S. agalactiae infections can cause sepsis, pneumonia, endocarditis, osteomyelitis, peritonitis and infections of the skin and connective tissues in immunocompromised individuals. Conditions that predispose adults to S. agalactiae infections are cancer, diabetes and HIV.

Fig1. Electrophoresis of PCR product by VetPCRTM STRE.AGAL Detection Kit

Culture-based methods are the most common test for detection and identification of S. agalactiae. They include hipurate hydrolysis, bile-esculin hydrolysis, bacitracin sensitivity and hemolysis and colony morphology on blood agar.

4. ORDERING INFORMATION

HumPCR™ STRE.AGAL Detection Kit is the direct detection of Streptococcus agalactiae on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : STRE.AGAL Positive sample Lane P : Positive control Lane N : Negative control

Product HumPCRTM STRE.AGAL Molecular Diagnostic HumPCRTM STRE.AGAL Detection Kit 48 or 96 BrigTM Molecular Weight Marker

Catalog No. HUM0082(S) HUM0082(48) HUM00782(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM STRE.PYO Detection Kit 2. SPECIMEN

Whole blood, pharyngeal and skin lesions swabs. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Streptococcus pyogenes are Gram positive, non-motile, facultatively anaerobic bacteria. They are spherical or ovoid in shape and occur in chains or pairs of cells. S. pyogenes is beta hemolytic in blood agar plates. This bacterium is found only in humans and is present in the throats of 20% of healthy children. It is usually transmitted from person to person via aerosols created from saliva or respiratory secretions. S. pyogenes attached to the pharyngeal mucosa via proteins M, protein F and lipoteichoic acid. The bacteria may simply replicate only sufficiently to maintain themselves without causing injury or may grow and secrete toxins, causing damage of the surrounding cells, invading the mucosa and eliciting an inflammatory response with pus formation. The person then has streptococcal pharyngitis. Sometimes the blood stream is invaded, resulting in septicemia or seeding to distant sites, with the developing of celulitis, fasciitis or myonecrosis.

HUMAN

Culture-based methods are the most common test for detection and identification of S. pyogenes. They include bacitracin sensitivity and hemolysis and colony morphology on blood agar. HumPCR™ STRE.PYO Detection Kit is the direct detection of Streptococcus pyogenes on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 490 bp M

P

1

2

3

N

500bp

490 bp

Fig1. Electrophoresis of PCR product by VetPCRTM STRE.PYO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : STRE.PYO Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM STRE.PYO Molecular Diagnostic HumPCRTM STRE.PYO Detection Kit 48 or 96 BrigTM Molecular Weight Marker

Catalog No. HUM0083(S) HUM008348) HUM00783(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM TCH.VAG Detection Kit 2. SPECIMEN

Vaginal, endocervical, or male urethral swab. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Thrichomonas vaginalis is an obligate anaerobic protozoan. The microorganism is pear-shaped, with a short undulating membrane lined with a flagellum and four anterior flagella. The size varies from 10 to 20 Οm. T. vaginalis has a worldwide distribution; it has been estimated that more than 180 million cases of trichomoniasis occur annually. This makes it the most common non-viral sexually transmitted disease worldwide. In females causes inflammation of the mucosal tissue of the vagina, vulva and cervix, accompanied by a copious, yellowish discharge. Less commonly, it affects the male urethra, prostate, and seminal vesicles, producing a white discharge. Diagnosis is made by direct detection of the organism or by laboratory culture. HumPCR™ TCH.VAG Detection Kit is the direct detection of Trichomonas vaginalis on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 323 bp M

P

1

2

3

N

Fig1. Electrophoresis of PCR product by VetPCRTM TCH.VAG Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : TCH.VAG Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM TCH.VAG Molecular Diagnostic HumPCRTM TCH.VAG Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

323 bp

300bp

Catalog No. HUM0084(S) HUM0084(48) HUM00784(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM TOXO.GO Detection Kit 2. SPECIMEN

Cerebrospinal fluid (CSF), whole blood, bone marrow, amniotic fluid. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Toxoplasma gondii is an obligate intracellular protozoan parasite that infects all warm-blooded vertebrates with a worldwide distribution. It causes a large range of clinical manifestations in humans. About one-third of the human population is chronically infected with this parasite, and infection is primarily caused by the ingestion of undercooked meat that contains viable T. gondii cysts or oocysts shed from the feces of infected cats. Although human infection with T. gondii is usually asymptomatic, cervical or occipital lymphadenopathy and ocular toxoplasmosis occurs in some patients. Congenital infection or reactivation in immunocompromised cases may lead to life-threatening encephalitis. HumPCRTM TOXO.GO Detection Kit is the direct detection of Toxoplasma gondii on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 462 bp M

N

1

2

3

P

500bp

462 bp

Fig1. Electrophoresis of PCR product by VetPCRTM TOXO.GO Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~3 : TOXO.GO Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM TOXO.GO Molecular Diagnostic HumPCRTM TOXO.GO Detection Kit 48 or 96

HUMAN

BrigTM Molecular Weight Marker

Catalog No. HUM0085(S) HUM0085(48) HUM00785(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM TRE.PALLI Detection Kit 2. SPECIMEN 1. DESCRIPTION

Treponema pallidum belongs to a family of spiral-shaped bacteria, the Spirochaetaceae (spirochetes). Is a Gram-negative spirochete measuring about 0.2 μm in width and 5-15 μm in length which causes a chronic sexually transmitted disease called syphilis. The World Health Organization estimates that 12 million new cases of syphilis occur each year. Syphilis is primarily sexually transmitted, but transmission by blood transfusion or via the placenta is possible. T. pallidum cannot be cultured in vitro. Diagnosis depends on the visualization of organisms using fluorescent or darkfield microscopy of smears from ulcer material, or on serology. HumPCR™ TRE.PALLI Detection Kit is the direct detection of Treponema pallidum on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

Swabs of chancres, whole blood, cerebrospinal fluid (CSF), amniotic fluid, aspirate and biopsy. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 514 bp M

N

1

2

3

4

P

500bp

514 bp

Fig1. Electrophoresis of PCR product by VetPCRTM TRE.PALLI Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~4 : TRE.PALLI Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM TRE.PALLI Molecular Diagnostic HumPCRTM TRE.PALLI Detection Kit 48 or 96

HUMAN

BrigTM Molecular Weight Marker

Catalog No. HUM0086(S) HUM0086(48) HUM00786(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM TRYP.CRUZY Detection Kit 2. SPECIMEN

Whole blood, cerebrospinal fluid (CSF). 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Trypanosoma cruzi is an obligate intracelular protozoan parasite that causes Chagas’ disease in humans and invades a great variety of mammalian cells. Infection with this parasite frequently involves the development of progressive pathology in tissues of the heart, esophagus and colon. Some people can be infected and never develop symptoms. For those who do, Chagas disease has three stages, acute infection, indeterminate stage and chronic infection, each with different symptoms. Chagas disease is usually spread by the feces of the triatomine bug, an insect that infests mud, adobe, or thatch houses. People get infected when they unknowingly rub bug feces into their eyes or mouth or into a bite wound. Infection can be also be transmitted by blood transfusions or organ transplants. The diagnosis of Chagas disease can be made by observation of the parasite in a blood smear by microscopic examination. This works well only in the acute phase of infection when parasites are seen circulating in blood. Diagnosis of chronic Chagas disease is generally made by testing with at least two different serologic tests. HumPCRTM TRYP.CRUZY Detection Kit is the direct detection of Trypanosoma cruzi on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 420 bp M

1

2

3

P

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM TRYP.CRUZY Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : TRYP.CRUZY Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM TRYP.CRUZY Molecular Diagnostic HumPCRTM TRYP.CRUZY Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

420 bp

Catalog No. HUM0087(S) HUM0087(48) HUM00787(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM TRYP.CRUZY Detection Kit 2. SPECIMEN

Urogenital swab or urine. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

U. urealyticum range in size from 0.2 to 0.8 Οm in diameter and are among the smallest of all free living organisms. Ureaplasma are difficult to culture because of their fastidious nutritional requirements and slow growth rates. This bacterium is a common comensal of the urogenital tract in humans. Also is the second most cause of nongonococcal urethritis in men and an opportunistic pathogen during pregnancy that can cause premature birth or spontaneous abort. HumPCR™ UR.UR Detection Kit is the direct detection of Ureaplasma urealyticum on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 415 bp M

1

2

3

P

N

400bp

415 bp

Fig1. Electrophoresis of PCR product by VetPCRTM UR.UR Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : UR.UR Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM UR.UR Molecular Diagnostic HumPCRTM UR.UR Detection Kit 48 or 96

HUMAN

BrigTM Molecular Weight Marker

Catalog No. HUM0088(S) HUM0088(48) HUM00788(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM UREA.PARV Detection Kit 2. SPECIMEN

Urogenital swab or urine. 1. DESCRIPTION 3. INTERPRETATION OF RESULTS

Ureaplasma parvum is a eubacteria belonging to the class Mollicutes. The lack of a rigid cell wall prevents them from staining by Gram stain, confers pleomorphism on their cells, and makes them very susceptible to dehydration, thereby limiting them to a parasitic existence in association with eukaryotic cells of their host. It is one of the smallest free living organisms known. U. parvum has been associated with the cause of various diseases. It has been categorized as a mucosal parasite living within the genito-urinary tracts. U. parvum can cause male urethritis, supperative arthritis, adverse pregnancy outcomes, chorioamnionitis, surgical wound infections, neonatal meningitis, pelvic inflammatory diseases, pyelonephritis, and neonatal disease. HumPCR™ UREA.PARV Detection Kit is the direct detection of Ureaplasma parvum on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 452 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM UREA.PARV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : UREA.PARV Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM UREA.PARV Molecular Diagnostic

Catalog No. HUM0090(S)

HumPCRTM UREA.PARV Detection Kit 48 or 96

HUM0090(48) HUM0090(96)

BrigTM Molecular Weight Marker

HUMAN

452 bp

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM VZV Detection Kit 2. SPECIMEN 1. DESCRIPTION

Skin scrapings, vesicular fluid, respiratory secretions, cerebrospinal fluid (CSF). 3. INTERPRETATION OF RESULTS

Varicella-zoster virus (VZV) is one of eight herpesviruses of the Herpesviridae family that are known to cause disease in people and some other primates. The virus is a DNA Îą-herpesvirus with a genome of about 125 000 bp that encode 70 genes. VZV is the causal agent of varicella (chickenpox) and herpes zoster (shingles). Varicella infection occurs in almost all people over their lifetimes. VZV becomes latent after varicella and usually persists silently and indefinitely. VZV reactivates, however, to cause zoster in roughly 20% of individuals, with higher reactivation rates in immunocompromised patients and the elderly. In most cases, the characteristic features of the vesicular varicella rash establish the clinical diagnosis. The diagnosis is made most definitively by demonstration of specific viral antigens in skin scrapings by immunofluorescence (DFA) using a commercial monoclonal antibody to VZV conjugated to fluorescein or by polymerase chain reaction (PCR). HumPCRTM VZV Detection Kit is the direct detection of Varicella-zoster virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 471 bp M

P

1

2

3

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM VZV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : VZV Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM VZV Molecular Diagnostic HumPCRTM VZV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

471 bp

Catalog No. HUM0091(S) HUM0091(48) HUM00791(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM DEN-1 Detection Kit 2. SPECIMEN

Whole blood, nasal swab, throat swab.

DESCRIPTION The Dengue virus type 1 is a member of the virus family Flaviviridae of which 50 other members, including West Nile and yellow fever viruses, have been identified. Dengue virus type 1 is a small virus that carries a single strand of RNA as its genome. The genome encodes only ten proteins. This virus is transmitted to people through the bite of the mosquitos Aedes aegypti and Aedes albopictus. Dengue virus is now believed to be the most common arthropod-borne disease in the world. Dengue fever is a disease caused by dengue virus type 1. The presence (the “dengue triad”) of fever, rash, and headache (and other pains) is particularly characteristic of dengue. Dengue hemorrhagic fever is a more severe form of the viral illness. This form of dengue fever can be life-threatening or even fatal. The diagnosis of dengue is usually made clinically and confirmed in the laboratory by serologic tests on blood samples from the patient.

HUMAN

HumPCRTM DEN-1 Detection Kit is the direct detection of Dengue virus type 1 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

3. INTERPRETATION OF RESULTS - Expected PCR product size : 193 bp M

N

P

1

2

3

200bp

193 bp

Fig1. Electrophoresis of PCR product by VetPCRTM DEN-1 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane P : Positive control Lane 1~3 : DEN-1 Positive sample 4. ORDERING INFORMATION Product HumPCRTM DEN-1 Molecular Diagnostic

Catalog No. HUM0001R(S)

HumPCRTM DEN-1 Detection Kit 48 or 96

HUM0001R(48) HUM0001R(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM DEN-2 Detection Kit 2. SPECIMEN

Whole blood, nasal swab, throat swab.

DESCRIPTION The Dengue virus type 2 is a member of the virus family Flaviviridae of which 50 other members, including West Nile and yellow fever viruses, have been identified. Dengue virus type 2 is a small virus that carries a single strand of RNA as its genome. The genome encodes only ten proteins. This virus is transmitted to people through the bite of the mosquitos Aedes aegypti and Aedes albopictus. Dengue virus is now believed to be the most common arthropod-borne disease in the world. Dengue fever is a disease caused by dengue virus type 2. The presence (the “dengue triad”) of fever, rash, and headache (and other pains) is particularly characteristic of dengue. Dengue hemorrhagic fever is a more severe form of the viral illness. This form of dengue fever can be life-threatening or even fatal. The diagnosis of dengue is usually made clinically and confirmed in the laboratory by serologic tests on blood samples from the patient.

HUMAN

HumPCRTM DEN-2 Detection Kit is the direct detection of Dengue virus type 2 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

3. INTERPRETATION OF RESULTS - Expected PCR product size : 235 bp M

1

2

3

P

N

300bp

235 bp

Fig1. Electrophoresis of PCR product by VetPCRTM DEN2 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : DEN-2 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM DEN-2 Molecular Diagnostic

Catalog No. HUM0002R(S)

HumPCRTM DEN-2 Detection Kit 48 or 96

HUM0002R(48) HUM0002R(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM DEN-3 Detection Kit 2. SPECIMEN

Whole blood, nasal swab, throat swab.

DESCRIPTION The Dengue virus type 3 is a member of the virus family Flaviviridae of which 50 other members, including West Nile and yellow fever viruses, have been identified. Dengue virus type 3 is a small virus that carries a single strand of RNA as its genome. The genome encodes only ten proteins. This virus is transmitted to people through the bite of the mosquitos Aedes aegypti and Aedes albopictus. Dengue virus is now believed to be the most common arthropod-borne disease in the world. Dengue fever is a disease caused by dengue virus type 3. The presence (the “dengue triad”) of fever, rash, and headache (and other pains) is particularly characteristic of dengue. Dengue hemorrhagic fever is a more severe form of the viral illness. This form of dengue fever can be life-threatening or even fatal. The diagnosis of dengue is usually made clinically and confirmed in the laboratory by serologic tests on blood samples from the patient.

HUMAN

HumPCRTM DEN-3 Detection Kit is the direct detection of Dengue virus type 3 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

3. INTERPRETATION OF RESULTS - Expected PCR product size : 275 bp M

P

1

2

3

N

275 bp

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM DEN-3 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane P : Positive control Lane 1~3 : DEN-3 Positive sample Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM DEN-3 Molecular Diagnostic

Catalog No. HUM0003R(S)

HumPCRTM DEN-3 Detection Kit 48 or 96

HUM0003R(48) HUM0003R(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HCV Detection Kit 2. SPECIMEN

Whole blood, nasal swab, throat swab.

DESCRIPTION Hepatitis C virus (HCV) is classified the genus Hepacivirus within the Flaviviridae family and has a positive-sense, single-stranded RNA genome of about 9.6 kilobases (kb). HCV is a major human health concern with an estimated 200 million people infected with HCV worldwide with resulting liver diseases including chronic hepatitis, cirrhosis, and hepatocellular carcinoma. The hepatitis C virus (HCV) is transmitted by blood-to-blood contact. In developed countries, it is estimated that 90% of persons with chronic HCV infection were infected through transfusion of unscreened blood or blood products or via injecting drug use or by inhalational drug use. In developing countries, the primary sources of HCV infection are unsterilized injection equipment and infusion of inadequately screened blood and blood products. The virus may be sexually transmitted, although this is rare. The available treatment options offer limited response rates. No HCV vaccines are available to date and only a subset of patients respond to current interferon-based treatment.

HUMAN

HumPCRTM HCV Detection Kit is the direct detection of Hepatitis C virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

3. INTERPRETATION OF RESULTS - Expected PCR product size : 614 bp M

N

1

2

3

4

P 614 bp

600bp

Fig1. Electrophoresis of PCR product by VetPCRTM HCV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane N : Negative control Lane 1~4 : HCV Positive sample Lane P : Positive control 4. ORDERING INFORMATION Product HumPCRTM HCV Molecular Diagnostic HumPCRTM HCV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

Catalog No. HUM0006R(S) HUM0006R(48) HUM0006R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HEV Detection Kit 2. SPECIMEN

DESCRIPTION The genus Enterovirus of the family Picornaviridae consists of over 100 mammalian and insect viruses. The viral genome, a single-stranded, (+)-strand RNA is enclosed in a nonenveloped capsid comprising 60 copies of four different polypeptides arranged with icosahedral symmetry. The bulk of Enterovirus infections are benign and are manifested by fever alone or, occasionally, present as distinct clinical syndromes such as hand-foot-mouth syndrome, herpangina, and pleurodynia. Enteroviruses also cause potentially severe and life-threatening infections such as meningitis, encephalitis, myocarditis, polio-like syndrome, and neonatal sepsis. Enterovirus infection may mimic bacterial disease and often leads to unnecessary antibiotic use and diagnostic testing until a bacterial disease has been excluded. The detection of Enterovirus by serology is of limited value clinically because it is slow, requiring acute and convalescent samples, and because of the large number of serotypes that exist. HumPCR™ HEV Detection Kit is the direct detection of Enterovirus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Cerebrospinal fluid (CSF), nasopharyngeal (NP)/throat swab, stool, rectal swab, or amniotic fluid. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 649 bp M

1

2

3

P

N

700bp

Fig1. Electrophoresis of PCR product by VetPCRTM HEV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HEV Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HEV Molecular Diagnostic HumPCRTM HEV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

649 bp

Catalog No. HUM0007R(S) HUM0007R(48) HUM0007R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HEV Detection Kit 2. SPECIMEN

DESCRIPTION The genus Enterovirus of the family Picornaviridae consists of over 100 mammalian and insect viruses. The viral genome, a single-stranded, (+)-strand RNA is enclosed in a nonenveloped capsid comprising 60 copies of four different polypeptides arranged with icosahedral symmetry. The bulk of Enterovirus infections are benign and are manifested by fever alone or, occasionally, present as distinct clinical syndromes such as hand-foot-mouth syndrome, herpangina, and pleurodynia. Enteroviruses also cause potentially severe and life-threatening infections such as meningitis, encephalitis, myocarditis, polio-like syndrome, and neonatal sepsis. Enterovirus infection may mimic bacterial disease and often leads to unnecessary antibiotic use and diagnostic testing until a bacterial disease has been excluded. The detection of Enterovirus by serology is of limited value clinically because it is slow, requiring acute and convalescent samples, and because of the large number of serotypes that exist. HumPCR™ HEV Detection Kit is the direct detection of Enterovirus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

Cerebrospinal fluid (CSF), nasopharyngeal (NP)/throat swab, stool, rectal swab, or amniotic fluid. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 649 bp M

1

2

3

P

N

700bp

Fig1. Electrophoresis of PCR product by VetPCRTM HEV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HEV Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HEV Molecular Diagnostic HumPCRTM HEV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

649 bp

Catalog No. HUM0007R(S) HUM0007R(48) HUM0007R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HIV-1 Detection Kit 2. SPECIMEN

DESCRIPTION

HUMAN

Human immunodeficiency virus (commonly known as HIV, and formerly known as HTLV-III and lymphadenopathy-associated virus) is a retrovirus that is the cause of the disease known as AIDS (Acquired Immunodeficiency Syndrome), a syndrome where the immune system begins to fail, leading to many life-threatening opportunistic infections. HIV primarily infects vital components of the human immune system such as CD4+ T cells, macrophages and dendritic cells. It also directly and indirectly destroys CD4+ T cells. As CD4+ T cells are required for the proper functioning of the immune system, when enough CD4+ T cells have been destroyed by HIV, the immune system functions poorly, leading to AIDS. HIV also directly attacks organs such as the kidneys, heart and brain, leading to acute renal failure, cardiomyopathy, dementia and encephalopathy. Many of the problems faced by people infected with HIV result from failure of the immune system to protect from opportunistic infections and cancers. HIV is transmitted through direct contact of a mucous membrane with a bodily fluid containing HIV, such as blood, semen, vaginal fluid, preseminal fluid or breast milk. Two species of HIV infect humans: HIV-1 and HIV-2. HIV-1 is hypothesized to have originated in southern Cameroon after jumping from wild chimpanzees (Pan troglodytes troglodytes) to humans during the twentieth century. HIV-2 is hypothesized to have originated from the Sooty Mangabey (Cercocebus atys), an Old World monkey of Guinea-Bissau, Gabon, and Cameroon. HIV-1 is more virulent, more easily transmitted and is the cause of the majority of HIV infections globally, while HIV-2 is less easily transmitted and is largely confined to West Africa. HumPCRTM HIV-1 Detection Kit is the direct detection of Human Immunodeficiency Virus type-1 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique..

Whole blood, cerebrospinal fluid (CSF), serum or plasm. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 231 bp M

1

2

3

P

N

300bp

231bp

Fig1. Electrophoresis of PCR product by VetPCRTM HIV-1 Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HIV-1 Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HIV-1 Molecular Diagnostic

Catalog No. HUM0008R(S)

HumPCRTM HIV-1 Detection Kit 48 or 96

HUM0008R(48) HUM0008R(96)

BrigTM Molecular Weight Marker

24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM MEA-V Detection Kit 2. SPECIMEN

DESCRIPTION

Nose and throat swabs, nasopharyngeal aspirates, cerebrospinal fluid (CSF). 3. INTERPRETATION OF RESULTS

Measles virus is a RNA virus with a genome of approximately 16 Kb, member of the family of Paramyxoviruses. Measles is one of the typical viral diseases of childhood. However, unlike other common viral diseases i.e. VZV, rubella, mumps, and parvovirus infections, measles often leads to severe complications that may be fatal. The virus spreads by the respiratory route via aerosol droplets and respiratory secretions which can remain infectious for several hours. The infection is acquired through the upper respiratory tract or conjunctiva. Measles typically begins with a mild to moderate fever, accompanied by other signs and symptoms, such as a persistent cough, runny nose, inflamed eyes (conjunctivitis) and sore throat. Two or three days later, Koplik’s spots (a characteristic sign of measles) appear. At the same time, a red blotchy rash appears. Complications are more common in children under the age of five or adults over the age of 20. The most serious complications include blindness, encephalitis (an infection that causes brain swelling), severe diarrhoea and related dehydration, ear infections, or severe respiratory infections such as pneumonia. HumPCRTM MEA.V Detection Kit is the direct detection of Measles virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only speciďŹ c gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

- Expected PCR product size : 586 bp M

1

2

3

P

N

300bp

Fig1. Electrophoresis of PCR product by VetPCRTM MEAV.V Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : MEA.V Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM MEAV.V Molecular Diagnostic HumPCRTM MEAV.V Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

231bp

Catalog No. HUM0010R(S) HUM0010R(48) HUM0010R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM ANDV Detection Kit 2. SPECIMEN

DESCRIPTION

Whole blood, serum or plasm. 3. INTERPRETATION OF RESULTS

Hantaviruses (HTVs) are rodent-borne negative-sense RNA viruses belonging to the Bunyaviridae family. In contrast to other Bunyaviridae, HTVs do not appear to have an arthropod vector, being spread by contact with rodents. HTV are the causative agents of hemorrhagic fever with renal syndrome (HFRS) and HTV pulmonary syndrome (HPS). Several human pathogenic strains of HTV have been identified worldwide. Several human pathogenic strains of HTV have been identified worldwide. The subtype Andes virus (ANDV) is responsible for most HPS in South America, Argentina and Chile. The major symptoms of this syndrome are fever, myalgia, headache, and gastrointestinal and cardiopulmonary dysfunction with a high case fatality rate. HumPCRTM ANDV Detection Kit is the direct detection of Hanta virus subtype Andes virus on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate and reliable technique.

- Expected PCR product size : 516 bp M

1

2

3

P

N

500bp

Fig1. Electrophoresis of PCR product by VetPCRTM ANDV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : ANDV Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM ANDV Molecular Diagnostic HumPCRTM ANDV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

HUMAN

516 bp

Catalog No. HUM0011R(S) HUM0011R(48) HUM0011R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)


HumPCRTM HIV Detection Kit 2. SPECIMEN

DESCRIPTION

HUMAN

Human immunodeficiency virus (commonly known as HIV, and formerly known as HTLV-III and lymphadenopathy-associated virus) is a retrovirus that is the cause of the disease known as AIDS (Acquired Immunodeficiency Syndrome), a syndrome where the immune system begins to fail, leading to many life-threatening opportunistic infections. HIV primarily infects vital components of the human immune system such as CD4+ T cells, macrophages and dendritic cells. It also directly and indirectly destroys CD4+ T cells. As CD4+ T cells are required for the proper functioning of the immune system, when enough CD4+ T cells have been destroyed by HIV, the immune system functions poorly, leading to AIDS. HIV also directly attacks organs such as the kidneys, heart and brain, leading to acute renal failure, cardiomyopathy, dementia and encephalopathy. Many of the problems faced by people infected with HIV result from failure of the immune system to protect from opportunistic infections and cancers. HIV is transmitted through direct contact of a mucous membrane with a bodily fluid containing HIV, such as blood, semen, vaginal fluid, preseminal fluid or breast milk. Two species of HIV infect humans: HIV-1 and HIV-2. HIV-1 is hypothesized to have originated in southern Cameroon after jumping from wild chimpanzees (Pan troglodytes troglodytes) to humans during the twentieth century. HIV-2 is hypothesized to have originated from the Sooty Mangabey (Cercocebus atys), an Old World monkey of Guinea-Bissau, Gabon, and Cameroon. HIV-1 is more virulent, more easily transmitted and is the cause of the majority of HIV infections globally, while HIV-2 is less easily transmitted and is largely confined to West Africa. HumPCRTM HIV Detection Kit is the direct detection of Human Immunodeficiency Virus type-1 and type-2 on the basis of a genetic database, so it can diagnose very fast and accurately. It can amplify only specific gene using the PCR (Polymerase Chain Reaction) method, and take only 3 hours for detection. Therefore, it is a very fast, accurate, reliable technique.

Whole blood, nasal swab, throat swab. 3. INTERPRETATION OF RESULTS - Expected PCR product size : 231 bp M

1

2

3

P

N

300bp

231 bp

Fig1. Electrophoresis of PCR product by VetPCRTM HIV Detection Kit Lane M : BrigTM Molecular Weight Marker (Bioingentech Ltda.) Lane 1~3 : HIV Positive sample Lane P : Positive control Lane N : Negative control 4. ORDERING INFORMATION Product HumPCRTM HIV Molecular Diagnostic HumPCRTM HIV Detection Kit 48 or 96 BrigTM Molecular Weight Marker

Catalog No. HUM0012R(S) HUM0012R(48) HUM0012R(96) 24012

BioingentechTM Genomic DNA Purification Kit (50 test)

230040(50)

BioingentechTM Genomic DNA Purification Kit (100 test)

230040(100)

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