http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105238790-B

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-113
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01K67-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-66
filingDate 2015-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105238790-B
titleOfInvention A kind of regulation and control pig AEBP1 promoter and construction method, transfection carrier and construction method, application
abstract The invention discloses a kind of regulation and control pig AEBP1 promoter and construction method, transfection carrier and construction method, application, the promoter is the deletion fragment of pig AEBP1 gene promoters.The present invention is studied pig AEBP1 promoter first, and by lacking the different fragments of the gene promoter, obtaining 3 kinds has more strongly active new promoter.The new promoter of the present invention can regulate and control the expression of pig AEBP1 genes, and new instrument and selection are provided for swine improvement.Biological experiment shows, 3 deleted carrier pGL3 basic Q1, pGL3 basic Q2, the pGL3 basic Q3 that the present invention is built have more strongly active, wherein pGL3 basic Q1 active highest in Ren sus domestica cell PK 15.The result of the present invention finally obtains 1483bp promoter fragment (337bp to 1819bp), i.e., the promoter fragment included in the deleted carrier pGL3 basic Q1 that the present invention is built, possesses independent startup function.
priorityDate 2015-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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