The test is a rapid colloidal gold immunochromatographic assay for the in vitro qualitative detection of the novel coronavirus(SARS-CoV-2), the influenza A virus (FluA) and the influenza B(FluB) antigen in human nasopharyngeal swab, oropharyngeal swab, nasal swab, and saliva samples from individuals suspected of respiratory viral infection.
The Treponema pallidum Antibody Assay Kit (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) to Treponema pallidum (Tp) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Tp.
The kit is used to qualitatively detect the novel coronavirus (SARS-CoV-2) nucleocapsid protein antigen in human nasal swab samples in vitro. In the acute phase of infection, antigens are usually detectable in upper respiratory tract specimens.
The kit is intended for the in vitro qualitative determination of Novel Coronavirus (2019-nCoV) IgG/IgM antibody in human serum, plasma or whole blood. Testing is limited to supplementary detection indicator for suspected nucleic acid negative results or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It should not be used as the basis for diagnosis and exclusion of Novel Coronavirus Pneumonia.
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