Competitive hog cholera virus antibody chemiluminescence quantitative detection kit
A technology for quantitative detection of swine fever virus, applied in chemiluminescence/bioluminescence, analysis through chemical reactions of materials, measurement devices, etc., can solve problems such as carcinogens, toxic substrates, and endogenous enzyme interference. It achieves the effects of low carcinogenicity and harm, short detection time and simplified operation process
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[0026] A kit for quantitative detection of swine fever virus antibody competition chemiluminescence, including antigen-coated plates, enzyme-labeled antibodies, calibrator, concentrated washing solution, luminescent substrate A, and luminescent substrate B;
[0027] The antigen-coated plate uses the purified CSFV E2 protein as the coated antigen, and uses pH9.6 carbonate buffer solution to coat the CSFV E2 protein on an opaque polystyrene plate;
[0028] The enzyme-labeled antibody is a monoclonal antibody against classical swine fever virus labeled with horseradish peroxidase by an enzyme-labeled antibody; the glutaraldehyde method is used for labeling, that is, the monoclonal antibody to classical swine fever virus, glutaraldehyde and horseradish peroxide The enzyme is added to the container for cross-linking, and the resulting mixture is dialyzed to remove excess glutaraldehyde; an equal volume of glycerol is added to the dialyzed mixture, and stored at -20°C;
[0029] For ...
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