The COVID-19 IgM/IgG Antibodies Rapid Test assay is a lateral flow immunoassay intended for qualitative detection and differentiation of IgM and IgG antibodies to COVID-19 in human serum, plasma (potassium EDTA), and venous whole blood.
The COVID-19 IgM/IgG Antibodies Rapid Test assay is intended as an aid in identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection.
The COVID-19 IgM/IgG Antibodies Rapid Test is for in vitro diagnostic use only and for professional use only.
Parameter of COVID-19 IgM/IgG Antibodies Rapid Test Kit (Colloidal Gold)
Material - pp
Test type - IgM/IgG Antibodies
Test method - Colloidal Gold
Specimen - Serum, plasma, or venous whole blood
Keep temperature - 2-30℃
Certification - CE, ISO 13485:2016
Shelf-life - 18 months
Package size - Carton Box, 1 pc/box, 5 pcs/box, 20 pcs/box,
rapid point-of -care diagnostic test
Simple. No instrumentation required&simple procedure
Accuracy. Highly sensitivity specificity and accuracy
Convenien. Suitable for large-scale use
This test is based on colloidal gold immunochromatography assay. During the test, specimens and detection buffer are applied to the test cartridges. If there are COVID-19 IgG or IgM antibodies in the specimens, they combine with colloidal gold-labeled COVID-19 recombinant antigen forming IgM-virus antigen-colloidal gold complex (complex M) or IgG-virus antigen-colloidal gold complex (complex G).
During lateral flow, the complex M and complex G move along the nitrocellulose membrane toward the end of the absorbent paper.