Hepatitis A virus antigen saliva fast detection test paper strip
A hepatitis A virus detection test strip technology, which is applied in measurement devices, resistance to vector-borne diseases, instruments, etc., can solve the problems of high detection cost and test strips not suitable for on-site detection, etc., and achieves high sensitivity and suitable for on-site detection. Detection and self-test, highly specific effect
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Embodiment 1
[0021] Preparation of colloidal gold pads
[0022] Prepare a colloidal gold solution with a diameter of 15nm by the chloroauric acid-trisodium citrate reduction method. After the preparation is completed, take 100ml of the colloidal gold solution in a beaker and use 0.1M K 2 CO 3 Adjust to pH 8.0, add 0.75 mg of corresponding polyclonal antibody against hepatitis A virus antigen (Shanghai Lingchao Biotechnology Co., Ltd.) to 100 ml of colloidal gold solution, stir at room temperature for 1 hour, add bovine serum white that is 5% by weight Protein (BSA) was blocked for 1 hour, centrifuged at 12000rpm, 4°C for 30 minutes, discarded the supernatant, redissolved with colloidal gold solution to 100ml, spread 22cm with 1ml solution 2 Spread the solution evenly on the glass fiber membrane and dry at 37°C for 30 minutes to make a colloidal gold pad.
[0023] Coating of nitrocellulose membrane
[0024] Dissolve the second monoclonal antibody against hepatitis A virus antigen (Shangh...
Embodiment 2
[0029] Preparation of colloidal gold pads
[0030] Prepare a colloidal gold solution with a diameter of 35nm by the chloroauric acid-trisodium citrate reduction method. After the preparation is completed, take 100ml of the colloidal gold solution in a beaker and use 0.1M K 2 CO 3 Adjust the pH to 8.2, add 1 mg of the corresponding first monoclonal antibody against hepatitis A virus antigen (Shanghai Lingchao Biotechnology Co., Ltd.) to the colloidal gold solution, stir at room temperature for 1 hour, add bovine serum white that is 5% by weight Protein (BSA) was blocked for 1 hour, centrifuged at 12000rpm, 4°C for 30 minutes, discarded the supernatant, redissolved with colloidal gold diluent to 100ml, spread 50cm with 1ml solution 2 Spread the solution evenly on the glass fiber membrane, and dry it at 37°C for 30 minutes to make a colloidal gold pad.
[0031] Coating of nitrocellulose membrane
[0032] Dissolve the second monoclonal antibody against hepatitis A virus antigen...
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