http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102359958-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0e6d51a03cd9e9c90ec65499716e2466
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-76
filingDate 2011-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8248e7c42063bd6555d68254ec301c0a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30255acbd56e9db1a48d6a848c214999
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_063492cb3167153b4ecae40e76ea1629
publicationDate 2013-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102359958-B
titleOfInvention Kit and method for detecting procalcitonin
abstract The invention discloses a kit for detecting procalcitonin. The kit comprises a luminous substrate, a magnetic particle coupling antibody, a biotinylation antibody and an enzyme marker, wherein the enzyme marker is horseradish peroxidase labeled streptavidin; and the antibody is a procalcitonin monoclonal antibody. In the kit, the magnetic particle coupling antibody is used as a fixed separation phase, a biotin-streptavidin multistage amplification system is adopted, the luminous substrate is catalyzed by using horseradish peroxidase serving as catalytic enzyme to emit light, and the detection sensitivity and accuracy of reagents are improved.
priorityDate 2011-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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