http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010540432-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-6459 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y304-21069 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-745 |
| filingDate | 2008-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2010-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2010540432-A |
| titleOfInvention | Purification method of human tissue type plasminogen activator |
| abstract | The present invention relates to an efficient and improved method for purifying recombinant proteins. The present invention relates to the purification of tissue plasminogen activator (tPA), such as truncated human tPA produced recombinantly in bacteria such as E. coli. The present invention provides a method that requires less refolding capacity after lysis of inclusion bodies isolated from cells expressing recombinant tPA without affecting the yield and purity of the tPA protein. The present invention also provides optimal arginine concentrations for use during protein refolding and during ion exchange chromatography. [Selection figure] None |
| priorityDate | 2007-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 99.