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Products Parameters PRINCIPLE AND PROCEDURE PRINCIPLE The membrane of the test device is coated with Rotavirus Group A antigen on the test region and goat anti rabbit IgG antibody on the control region. Lable pad are coated by fluorescence labeled anti Rotavirus Group A and rabbit IgG in advance. When testing positive sample, the RV in sample combine with fluorescence labeled anti Rotavirus Group A, and form immune mixture. Under the action of the immunochromatography, the complex flow in t... -
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Products Parameters PRINCIPLE AND PROCEDURE PRINCIPLE The membrane of the test device is coated with anti PSA antibody on the test region and goat anti rabbit IgG antibody on the control region. Lable pad are coated by fluorescence labeled anti PSA antibody and rabbit IgG in advance. When testing positive sample, the PSA antigen in sample combine with fluorescence labeled anti PSA antibody, and form immune mixture. Under the action of the immunochromatography, the complex flow in the direct... -
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FOB Brochure PRINCIPLE AND PROCEDURE OF FOB TEST Princple: The strip has anti-FOB coating antibody on test region, which is fastened to membrane chromatography in advance. Lable pad is coated by fluorescence labeled anti-FOB antibody in advance. When testing positive sample, the FOB in sample can be mixed with fluorescence labeled anti-FOB antibody, and form immune mixture. As the mixture is allowed to migrate along the test strip, the FOB conjugate complex is captured by anti-FOB coating ... -
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Diagnostic Kit for Myoglobin (fluorescence immunochromatographic assay) For in vitro diagnostic use only Please read this package insert carefully prior to use and strictly follow the instructions. Reliability of assay results cannot be guaranteed if there are any deviations from the instructions in this package insert. INTENDED USE Diagnostic Kit for myoglobin (fluorescence immunochromatographic assay) is a fluorescence immunochromatographic assay for the quantitative detection the concent... -
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SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)is intended for the qualitative detection of SARS-CoV-2 Antigen(Nucleocapsid protein) in nasal swab specimens in vitro.The positive results indicate the existence of SARS-CoV-2 antigen. It should be further diagnosed by combining the patient’s history and other diagnostic information[1]. The positive resultsdo not exclude bacterial infection or other viral infection. Pathogens detected are not necessarily the main cause of disease symptoms. ... -
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