http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102747082-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c6d22af4bf4e1b2205a929549da46d3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01K67-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-113
filingDate 2011-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18fb12a3c05af6ffc8ccea054f3a8c2f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_050ae991fd3ce8a950a2a6ebf6a4ca80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70689b9e073c752b87b7e18b195ba1d7
publicationDate 2014-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102747082-B
titleOfInvention Pig muscle-specific ITGB1BP2 promoter and application thereof
abstract The present invention belongs to the field of pig molecule genetics, and specifically relates to cloning identification of a pig muscle-specific expression gene integrin beta 1 binding protein 2 (ITGB1BP2) promoter, and an application thereof. The steps of the present invention comprise: extracting total RNA of different tissues of a large white pig, and carrying out fluorescence quantitative PCR to determine specific expression in muscle tissue. According to the present invention, the total DNA of the muscle tissue of the large white pig is adopted as a template to design primers; PCR amplification is performed to obtain a 1442 bp sequence of flank on 5' terminal of pig ITGB1BP2 gene; luciferase reporter gene plasmids of 15 ITGB1BP2 promoter deletion fragments with different lengths are constructed; and C2C12 cells are transfected with the plasmids, activity of the promoter of each deletion fragment is detected, and the pig ITGB1BP2 gene promoter is identified. The nucleotide sequence of the pig ITGB1BP2 gene promoter of the present invention is represented by SEQ ID NO:1. With the present invention, import elements and means are provided for pig genetic improvement and transgene, and muscle tissue specificity and stability of transgene expression can be strengthened.
priorityDate 2011-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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