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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2f70f4729a5349e37218e21fe5a7d24a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 2011-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea45e994566b9955be5b8b1d304d3d49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a4c94880235efa79ea51ecf899dbe95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_712e06dca89959a1a100537616e8a4f3
publicationDate 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102323409-B
titleOfInvention Virus infection detection method
abstract The invention discloses a virus infection detection method. The virus infection detection method comprises the following steps of: (1) coupling a viral reactogenicity polypeptide to a non-protein polymer to obtain a coupled polypeptide; and (2) adding the coupled polypeptide in a coating liquid, then adding a serum sample (to be detected) to perform the ELISA (enzyme-linked immunosorbent assay) detection, judging the virus and subtype infection thereof according to an immunoadsorption reaction. The detection method provided by the invention can obviously improve the detection sensitivity as well as obviously reduces the non-specific background readout, has high specificity, simplicity in operation, rapidness in diagnosis speed, and is economic and convenient in large scale detection; and the detection method is a good method easy for popularization and wide in application prospect. In the detection provided by the invention, the dosage of the coating antigen can be 10 ng/ml, and the less dosage is in favor of popularization and application.
priorityDate 2011-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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