http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105838826-B

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-701
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686
filingDate 2016-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105838826-B
titleOfInvention Double-color fluorescent PCR primer, probe and method for rapidly distinguishing canine parvovirus vaccine strain and wild strain
abstract The invention discloses a bicolor fluorescent PCR primer, a probe and a method for rapidly distinguishing a canine parvovirus vaccine strain and a wild strain. The method combines a real-time fluorescence PCR technology and a melting curve analysis technology, and identifies the canine parvovirus vaccine and the wild strains according to the melting curve peak type and the Tm value difference; the operation is simple: only one reaction is needed to realize the identification and detection of three genotype wild strains and two vaccines; the detection speed is high and the flux is high: 3 hours are not needed in the whole operation process, cell culture of the virus is not needed, and the time for identifying and detecting three different genotypes of the virus and two vaccines and wild strains is greatly shortened; the method has the advantages of high accuracy, good specificity and good repeatability, can accurately, quickly and highly-flux analyze, and is favorable for popularization and application in clinical practice.
priorityDate 2016-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 19.