http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110551853-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-701
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-93
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70
filingDate 2019-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110551853-B
titleOfInvention Triple PCR detection primer and kit for rapidly distinguishing African swine fever virus wild strain and gene deletion strain
abstract The invention discloses a triple PCR detection primer group for rapidly distinguishing African swine fever virus wild strains from CD2V and/or 360-fold 505R gene deletion strains, wherein the nucleotide sequences of three pairs of detection primers are shown as SEQ ID NO: 1 to 6. The invention utilizes three pairs of primers to amplify three genes of African swine fever virus CD2V, P72 and 360-one 505R at one time, thus reducing the detection cost and the detection time for identifying different genes; and three genes with different lengths can be amplified by only one PCR reaction, and whether the genes are deleted or not in the strain is distinguished. Three genes can be identified only by one-time PCR amplification, and for a sample for respectively amplifying and detecting the three genes by using the traditional method, the cost is reduced by about 2/3, and the method has a wide market prospect.
priorityDate 2019-09-19-04:00^^<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: 21.