Use method of immunochromatographic kit for rapidly detecting novel coronavirus N protein
A coronavirus and immunochromatography technology, applied in immunoassays, measuring devices, analytical materials, etc., can solve problems such as insufficient to fully meet the needs of epidemic prevention and control, restrict the supply capacity of new coronavirus rapid detection services, and accelerate the epidemic. The effect of screening suspected cases on the front line, reducing social panic, and simple operation
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Embodiment 1
[0038] 1. Preparation of novel coronavirus N protein immunochromatographic detection kit
[0039] 1) Use fluorescent microspheres to label another strain of mouse anti-new coronavirus N protein monoclonal antibody
[0040] Take 0.5mL fluorescent microspheres, add 1mg carbodiimide (EDC), 1mg N-hydroxysuccinimide (NHS), stir at room temperature, 120r / min for 3h, then add 100μL of another strain of mouse anti-new coronavirus For virus N protein monoclonal antibody, stir for 1 hour at room temperature at a speed of 120 r / min, then add 10 mg of BSA blocking solution, and continue stirring for 1 hour at a speed of 120 r / min. Centrifuge at 12000 r / min for 20 min at 2-8 °C, and remove the supernatant. Finally, the solid precipitate obtained after centrifugation was redissolved to 1 mL with 0.2 M phosphate buffer (pH=7.4), and then 1 μL of Proclin300 was added and stored at 4°C until use.
[0041] 2) Using fluorescent microspheres to label rabbit IgG polyclonal antibody
[0042] Tak...
Embodiment 2
[0071] Serum / Plasma / Whole Blood Sample Testing
[0072] The types of samples taken include serum / plasma / whole blood.
[0073] After the serum / plasma / whole blood sample is collected, no sample pretreatment is required, and the sample to be tested is directly added dropwise to the sample inlet of the test card and allowed to stand for 15 minutes, and then inserted into the fluorescence immunochromatography analyzer for detection, the instrument automatically calculates the sample T / C value, judge negative or positive by comparing with normal value range. In addition, when two fluorescent bands appear under ultraviolet light irradiation, it is positive. The clinical test results are shown in Table 5 below.
[0074] table 5
[0075]
[0076]
[0077] As can be seen from the clinical testing data in Table 5, all the 20 negative samples were detected as negative, which was consistent with the clinical diagnosis; all the 20 positive samples were detected as positive, and the...
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