For professional use only
Minimum Order Quantity of 50.000 test.
Rapid Anti-HCV Test is a colloidal gold enhanced rapid immunochromatographic assay for qualitative detection of antibodies to hepatitis C virus (HCV) in human whole blood (venous and fingerstick), serum or plasma. The test is intended for healthcare professionals and trained healthcare workers to use as an aid for diagnosis.
Sub-distributors in Europe welcome! Prices listed are for single orders. Volume pricing upon request, send us a message (info@prodiag.nl).
InTec Products Inc. HIV rapid test is supplied in a complete Point-of-Care package to perform 10 tests.
The High Risk HPV Genotyping Kit (Abbreviation: Sanity 2.0 hrHPV) is a qualitative in vitro test used for HPV genotyping and cervical cancer screening using cervical cells collected by swab, TCT or LCT. This test utilizes Polymerase Chain Reaction (PCR) for DNA amplification and nucleic acid hybridization for the detection of high-risk HPV types in one reaction. This test specifically identifies 14 high-risk HPV types, including HPV-16, HPV-18, HPV-31, HPV-33, HPV-35, HPV-39, HPV-45, HPV-51, HPV-52, HPV-56, HPV-58, HPV-59, HPV-66, and HPV-68.
The HPV DNA extraction kit (Sanity 2.0) utilizes magnetic particle technology for automated isolation and purification of nucleic acid from cervical secretions.
MTB DNA Extraction Kit (for the Sanity 2.0) utilizes magnetic particle technology for automated isolation and purification of nucleic acid from sputum sample, Tuberculosis cultured sample, Bronchial washing fluid, Bronchoalveolar lavage fluid (BALF) sample etc.
The MTB Test Kit (for use on the Sanity 2.0 system) is a cartridge-based test kit for qualitative detection of Mycobacterium tuberculosis complex (MTBC) in sputum specimens.
The Mycobacteria Identification Kit (Sanity 2.0) (Abbreviation: Sanity Myco) is a cartridge-based test kit for identifying 19 clinically relevant mycobacteria (including M. tuberculosis complex, M. chelonae, M. scrofulaceum, M. bovis, M. smegmatis, M. abscessus, M. kansasii, M. gordonae, M. lentiflavum, M. simiae, M. nonchromogenicum, M. terrae, M. marinum/M. ulcerans, M. fortuitum, M. avium, M. intracellulare, M. xenopi, M. malmoense and M. szulgai) from sputum samples.
The MDR-TB Test Kit (Sanity 2.0) (Abbreviation: Sanity MDR-TB) is a cartridge-based test kit for detecting multidrug-resistance mutations (including rifampin-resistant mutations and isoniazid-resistant mutations) in Mycobacterium tuberculosis (MTB) from sputum samples.
Sanity 2.0-Pathogen Nucleic Acid Extraction Kit can purify nucleic acid from saliva, bronchoalveolar lavage fluid (BALF), sputum, swab sample, etc.
This kit is used for in vitro qualitative detection of novel coronavirus (SARS-CoV-2) ORF1ab and N gene in specimens, including nasopharyngeal swab, oropharyngeal swab, saliva, sputum, bronchoalveolar lavage fluid, for diagnosis of the COVID-19 infection, the suspected cluster cases and of the patients who need differential diagnosis of COVID-19 infection.
The Sanity 2.0 Respiratory Pathogen Panel RPP12 is a multiplex real-time, reverse transcriptase polymerase chain reaction (RT-PCR) test intended for the in vitro qualitative detection and differentiation of viral RNA in nasopharyngeal swab (NPS), oropharyngeal swab (OPS) and sputum specimens obtained from individuals suspected of respiratory tract infections.
Point of care (POC) qPCR with integrated, complete extraction: the Sanity 2.0 is the ideal POC qPCR for small-scaled labs. The Sanity can be used for multiple purposes, including the identification of several respiratory diseases (SARS-CoV-2, Influenza, RSV), Tuberculosis and HPV.
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