http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103409359-B

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-705
filingDate 2013-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2015-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103409359-B
titleOfInvention Application in the prokaryotic expression bacterial strain of TREM-1 extracellular domain and the septicemia that causes at treatment streptococcus suis infection
abstract The invention belongs to biological technical field, be specifically related to a kind of prokaryotic expression bacterial strain of TREM-1 extracellular domain and the application in the septicemia that causes for the treatment of streptococcus suis infection.A prokaryotic expression bacterial strain for TREM-1 extracellular domain, is characterized in that: called after Escherichia? coil? BL21/PET28a-TREM1, does is its preserving number: CTCC? M? 2013272.When bacterial strain BL21/pET28a-TREM1 expresses mouse TREM-1 protein ectodomain, TREM-1 protein ectodomain carries simultaneously FLAG and HIS two labels.Apply the affine resin of FLAG and NTA resin and FLAG and HIS two labels and successively purifying is carried out to obtained albumen, and carry out intracellular toxin process.Highly purified TREM-1 extracellular domain recombinant expression protein can be obtained, its high purity more than 90%.<!--1-->
priorityDate 2013-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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