Intec SARS-CoV-2 Antigen Testing kit – Covid19 Self-Test kit

InTec SARS-CoV-2 Antigen Rapid Test for the rapid and qualitative determination of SARS-CoV-2 infection from swab specimens. This latest version InTec Rapid SARS-CoV-2 Antigen Test can be used with either nasopharyngeal or (undeep) nasal swab samples. The test contains a prefilled buffer solution which makes product handling even easier. Apart from being put on many recommendation lists, the test has also been validated in a prospective validation study performed by Microbe & Lab in the Netherlands, this study showed that even in a mild symptomatic patient population, the test passes the WHO criteria.

The Rapid SARS-CoV-2 Antigen Test is a colloidal gold-enhanced, rapid immunochromatographic assay for the qualitative detection of SARS-CoV-2 antigens in the nasopharyngeal specimen collected by the swab from individuals who are suspected of COVID-19 by healthcare professionals and trained health care workers as an aid in the diagnosis of SARS-CoV-2 infection. The test is suitable for use in hospitals, clinics, testing laboratories, and other medical facilities.

The SARS-CoV-2 Rapid Antigen Test (Colloidal Gold Method) is intended for the qualitative

detection of the SARS-CoV-2 nucleocapsid protein in human nasopharyngeal or nasal swab

This kit is intended for rapid and qualitative determination of SARS-CoV-2 infection from swab specimens. Antigens of SARS-CoV-2 in the specimens are allowed to react with the anti-SARS-CoV-2 monoclonal antibody-coupled gold conjugate followed by reaction with anti-SARS-CoV-2 monoclonal antibodies immobilized in the test line. When the sample contains SARS-CoV-2 antigens, a visible line appears in the test region on the membrane. The solution continues to migrate to encounter a control reagent that binds a control conjugate, thereby producing another band in the control region.

The test is very easy to use and the results are shown within 15-20 minutes!
This latest version InTec Rapid SARS-CoV-2 Antigen Test can be used with either nasopharyngeal or (undeep) nasal swab samples: