http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114705856-A

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filingDate 2022-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2022-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114705856-A
titleOfInvention Method, reagent and kit for detection of antigen content of delta variant strain in novel coronavirus vaccine
abstract The embodiment of the present invention discloses a method for detecting the antigen content of a delta variant strain in a novel coronavirus vaccine, comprising: preparing a goat polyclonal antibody against the S protein receptor binding region (RBD) epitope of the novel coronavirus delta variant strain Coat the enzyme-labeled plate, seal the enzyme-labeled plate, wash the plate, and pat it dry; add the vaccine antigen sample to be tested and the antigen standard substance respectively, and dilute them in different gradients in the plate, and then add the antigen sample of the vaccine to be tested and the antigen standard. The ELISA plate of the antigen standard was sealed and incubated at 37°C for 1 h to 2 h, washed and patted dry; a rabbit polyclonal antibody against the epitope of the S protein receptor binding region of the new coronavirus delta variant was added as the primary antibody, and the The enzyme-labeled plate containing the primary antibody was sealed and incubated at 37°C for 1 h to 2 h, washed and patted dry; goat anti-rabbit Ig antibody labeled with horseradish peroxidase was added as the secondary antibody at an appropriate dilution to obtain a secondary antibody containing the primary antibody. After the plate was sealed and incubated at 37°C for 1 h to 2 h, the plate was washed; after adding a chromogenic solution for color reaction, the antigen content of the vaccine antigen sample to be tested was determined. The invention can significantly increase the antigen content of the delta variant strain in the new crown vaccine.
priorityDate 2022-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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