http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2605149-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-06
filingDate 2006-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be9ca65fa7a31f96a22200b1b8b51975
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0faef93cd4e3ff723c40d266bd8634a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5921266c97495f0b677171ca24b1874c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_961d86ec429b675639d5a6fe89f09c91
publicationDate 2006-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2605149-A1
titleOfInvention Production of recombinant proteins by autoproteolytic cleavage of a fusion protein
abstract Disclosed is a method for the production of a heterologous polypeptide of interest with a homogenous N-terminus, using a fusion polypeptide comprising the polypeptide of interest and N-terminally thereto a polypeptide exhibiting autoproteolytic function, said method comprising the steps of a) binding of the fusion polypeptide in a soluble, autoproteolytically inactive form by an affinity chromatography system, b) refolding of the fusion polypeptide, thereby activating the autoproteolytic function of the fusion polypeptide and causing cleavage of the heterologous polypeptide of interest, and c) subsequently eluting the heterologous polypeptide of interest, wherein said steps are conducted on one affinity chromatography system.
priorityDate 2005-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP01331
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP37885
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Total number of triples: 443.