The reagent can be used for quantitative determination of C-reactive protein and serum amyloid A in human serum, plasma or whole blood samples in vitro. For auxiliary diagnosis.

1. Take out the test card from the aluminum foil packaging bag and place it on a horizontal and dry surface.            

2. Insert the IC card into the fluorescence analyzer, click to read the IC card, confirm that the batch number of the IC card and the detection card match, and calibrate the IC card (see the instrument manual for details)            

3. Suck 5 μ l serum / plasma (or 8.5 μ l whole blood sample) into buffer solution, mix well for 30 seconds, suck 100 μ l into test card            

4. After 15 minutes, insert the detection card into the card slot of the applicable instrument, and conduct quantitative interpretation of the results.

The contents of C-reactive protein and serum amyloid A in human serum, plasma or whole blood samples were detected by fluorescence quantitative immunochromatography. When the sample is dropped into the sample hole of the test card, SAA, CRP in the sample combine with the anti SAA monoclonal antibody and CRP monoclonal antibody labeled with fluorescent substances in the reagent pad to form a reaction complex. The reaction complex moves forward along the nitrocellulose (NC) membrane along with the chromatography, and is captured by the corresponding monoclonal antibody on the nitrocellulose (NC) membrane detection line The content of SAA and CRP in the sample was detected by fluorescence analyzer.