http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102841203-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4fb38ebd40c70e97cc5f1519c6699162
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-545
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D313-00
filingDate 2012-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c64dd55d77cb3badb4a24c9959eb3d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e498c35985100a2b41eed3c7a88bd40
publicationDate 2014-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102841203-B
titleOfInvention Competitive ELISA (enzyme-linked immuno sorbent assay) non-toxic detection method for zearalenone (ZEN)
abstract The invention discloses a competitive ELISA (enzyme-linked immuno sorbent assay) non-toxic detection method for zearalenone. The method disclosed by the invention is a competitive ELISA method built by ZEN-BSA (zearalenone-bovine serum albumin), a ZEN monoclonal antibody and a beta-anti-idiotype monoclonal antibody of ZEN. A ZEN standard substance is replaced by the beta-anti-idiotype monoclonal antibody of ZEN, so as to avoid the damage of toxin to an operator and the possibility of scattering toxin to the environment, and non-toxic detection is achieved. According to the method, the ZEN standard substance is not needed, so that the cost can be greatly reduced; and zearalenone polluted by foods, grains, feed and the like can be rapidly and sensitively detected at a large scale, therefore, the method has a good market prospect.
priorityDate 2012-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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