Immune chromatography reagent kit for screening multiple great infectious diseases simultaneously
A technology of immunochromatography and reagent kits, which is applied in the direction of analysis materials, measuring devices, instruments, etc., can solve the problems of long detection time, waste of manpower and material resources, inconvenient and fast, etc., and achieve the effect of shortening the window period and saving costs
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Embodiment 1
[0055] Example 1 Coating of Antigen and Antibody
[0056] Dilute HBsAg monoclonal antibody, HCV antigen, HIV antigen, HIV P24 monoclonal antibody, and TP antigen to appropriate concentrations, and draw them on the NC membrane with a film-drawing instrument, that is, HBV, HCV, HIV (including HIV P24Ag), TP Five detection lines. Dilute the quality control line antibody goat anti-rabbit IgG antibody to the optimum concentration and draw it on the NC membrane with a film-drawing instrument, which is the control line. Place the scratched NC film in a 37-degree incubator to dry for half an hour.
Embodiment 2
[0057] Example 2 Preparation of colloidal gold
[0058] Get 100ml of ultrapure water in a 500ml round bottom flask, put it on a heating stirrer and heat to boiling, add 1ml of 1% aqueous solution of chloroauric acid (Sigma-Aldrich, U.S.), add 0.5ml of 1% sodium citrate after boiling (U.S. Sigma-Aldrich Company), continue to heat for 10 minutes and place it to cool naturally, which is colloidal gold.
Embodiment 3
[0059] Example 3 Preparation of Colloidal Gold-Marker
[0060] Take 10ml of HBsAg monoclonal antibody and put it into a dialysis bag, dialyze against 10mM PBS pH 7.4 buffer solution for 8 hours, during which the buffer solution is changed every 1 hour. Take 10ml colloidal gold, with 0.2M K 2 CO 3 Adjust the pH of the colloidal gold solution to 6-7, add 200ug HBsAg monoclonal antibody, and continue stirring for 5-10 minutes. Add 0.5 ml of 2% BSA solution to the above mixture, and continue stirring for 5 minutes. Put the above mixture into a suitable centrifuge tube. Centrifuge at 5000rpm for 10 minutes, suck out the supernatant, and collect the precipitate into a suitable container; centrifuge the supernatant at 10000rpm for 15 minutes, repeat the first centrifugation operation; centrifuge the supernatant at 12000rpm for 30 minutes, discard the supernatant, Collect the three centrifuged precipitates into the same centrifuge tube, dilute to 1ml with colloidal gold diluent, a...
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