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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-124
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6888
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6888
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
filingDate 2019-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110628919-B
titleOfInvention Method for detecting g. +6723 locus genotype of sheep MSTN gene
abstract The invention discloses a method for detecting g. +6723 locus genotype of a sheep MSTN gene, belonging to the technical field of genetic engineering and genetic breeding. Compared with the traditional method for detecting the g. +6723 site genotype of the sheep MSTN gene based on 4P-ARMS-PCR, PCR-RFLP, PCR-SSCP and Sanger sequencing, the method disclosed by the invention is based on a specific primer pair and high-resolution melting curve analysis, so that the method disclosed by the invention can be used for typing the three genotypes AA, AG and GG at the g. +6723 site of the sheep MSTN gene only by means of one-time PCR without enzyme digestion or sequencing and the like, and is extremely high in detection efficiency and simple and convenient to operate.
priorityDate 2019-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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