Chemiluminescent examining method for insulin content and C-peptide content in human blood serum
A chemiluminescence detection and human serum technology, applied in the field of clinical blood immunodetection, can solve the problems of affecting the health and quality of life of patients, difficult to eliminate interference, inconvenient clinical use, etc., to achieve improved specificity, no radioactive pollution, and easy operation. Effect
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[0025] Example, (1) Preparation of a quantitative detection kit for human serum insulin:
[0026] 1. Coating plate production: use PH7.4 Tris-HCl buffer as the coating buffer, add 4ug / ml of monoclonal antibody, coat according to 100ul / well, 37°C for 3 hours and 4°C overnight, then shake off the liquid , Wash with washing solution, use 1% bovine serum albumin (BSA-PBS)-2.5% sucrose (0.01M, PH=7.4) as the blocking solution, and block overnight at 4°C.
[0027] 2. Antibody labeling:
[0028] 1) Dissolve 12 mg of horseradish peroxidase in 3 ml of freshly prepared deionized water.
[0029] 2) Add 0.1mol / L sodium periodate solution according to 51ul / 1mg enzyme, mix well, and activate at 4°C for 60 minutes.
[0030] 3) Add ethylene glycol according to 26ul / 1mg enzyme, mix well, react for 30 minutes at 4°C to terminate the reaction.
[0031] 4) Put the above reaction mixture into a dialysis bag, dialyzed against 1mmol / L acetic acid buffer, 4°C overnight, and change the dialysate 2-3 times...
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