Competitive ELISA detection method for DHAV-1 antibodies
A technology for duck hepatitis A virus and a detection method, which is applied in the field of ELISA detection of type 1 duck hepatitis A virus antibody competition, can solve the problems of difficulty in evaluating the titer of DHAV-1 egg yolk antibody, and achieve the effects of good stability and high specificity.
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[0043] This example provides a competitive ELISA detection method for initially establishing a DHAV-1 antibody using a monoclonal antibody.
[0044] ①The monoclonal antibody 3B2 was labeled with horseradish peroxidase (HRP). After the monoclonal antibody was purified by the conventional caprylic ammonium sulfate method, the purity of the monoclonal antibody was identified by SDS-PAGE. After the concentration of the monoclonal antibody was determined, the monoclonal antibody was labeled with horseradish peroxidase by the simple sodium periodate method.
[0045] ② Determine the coating concentration of antigen VP1 protein and the optimal dilution concentration of enzyme-labeled antibody by square array test, and determine the optimal dilution concentration of detection serum by calculating the inhibition rate of positive serum and negative serum. The established competitive ELISA method was used to detect the sample serum, and the critical value of the detection method was dete...
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