De Anti-HCV Sneltest is een colloidal gold immunochromatografische assay voor de kwalitatitieve bepaling van antilichamen tegen het Hepatitis C Virus (HCV) in humane bloed samples (veneus bloed vanuit vingerprik), serum of plasma. De test is bedoeld voor professioneel gebruik.
InTec Products Inc. HIV rapid test wordt geleverd in een complete Point-of-Care verpakking waarmee 10 testen uitgevoerd kunnen worden.
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 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.
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 Sanity 2.0 Respiratory Pathogen Panel is a multiplex real-time, reverse transcriptase polymerase chain reaction (RT-PCR) test intended for the in vitro qualitative detection and differentiation of influenza A, influenza B, respiratory syncytial virus (RSV) viral RNA in nasopharyngeal swab (NPS), oropharyngeal swab (OPS) and sputum specimens obtained from individuals suspected of respiratory tract infections.
The kit is only used for in vitro diagnosis by professionals. It is used for rapid identification of SARS-CoV-2 variant Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2) and B.1.617.1 / B.1.617.3 and qualitative detection of SARS-CoV-2 in samples including nasopharyngeal swab, oropharyngeal swab, saliva, bronchoalveolar lavage fluid and sputum.
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.
Getoonde prijzen zijn voor losse bestellingen. Medische professionals en grote afnemers kunnen prijzen opvragen via ons e-mailadres (info@prodiag.nl).
De InTec SARS-CoV-2 Antigen Rapid Test: voor een snelle en kwalitatieve bepaling van een SARS-CoV-2 (corona) infectie uit swab samples. Deze nieuwste versie van de InTec SARS-CoV-2 Antigen Rapid Test kan worden gebruikt voor zowel diepe nasofaryngeale als ondiepe neus swab samples. De test bevat een voorgevulde bufferoplossing, dit maakt het nog makkelijker om de test uit te voeren! Naast het feit dat de test is toegevoegd aan vele aanbevelingslijsten, is de test ook gevalideerd door Microbe & Lab, deze validatie studie laat zien dat zelfs met milde klachten de test nog steeds aan de WHO criteria voldoet.
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