http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006025577-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c1818a6531b2b488f5cb4b06281b3beb http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0d54c6b08608c592b6bae2f5dda72dee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a27a452f0808b64493aae5bbf7becce6 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-1866 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-52 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-59 |
filingDate | 2005-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_147bec605dc83316d0da47da80b96f8f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ddd1362c40c2b54ad20db30e0e5e984 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c78e715d628d04d28fb468700f4a979 |
publicationDate | 2006-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-2006025577-A1 |
titleOfInvention | Endothelial cell growth factor methods of isolation and expression |
abstract | A novel growth factor specific for vascular endothelial cells has been identified in conditioned medium of bovine pituitary derived folliculo stellate cells. This factor, named folliculo stellate derived growth facto (FSdGF) or vascular endothelial growth factor (VEGF), was purified to homogeneity by a combination of heparin sepharose affinity chromatography, Bio Gel P-60 exclusion chromatography, Mono S ion exchange chromatography and hydrophobic chromatography on a C4 reverse phase HPLC column. The factor is also found in the murine AtT-20 cell line. Alternatively, the growth factor is purified by a first reverse phase HPLC using acetonitrile gradient followed by a second reverse phase HPLC using an isopropanol gradient. FSdGF, having a molecular weight of about 43,000 da, was characterized as a glycoprotein composed of two homologous sub units with MW of about 23 kDa. FSdGF was a potent mitogen for vascular endothelial cells with activity detectable at 10 pg/ml and saturation at 500 pg/ml. It did not stimulate the proliferation of other cell types such as bovine corneal endothelial cells, adrenal cortex cells, granulosa cells, BALB/MK cells or BHK-21 cells. Microsequencing revealed an amino terminal sequence containing no significant homology to any known protein. The release of FSdGF by pituitary cells and its unique target cell specificity indicate that FSdGF is useful in angiogenesis. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007021342-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006287234-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10443032-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10493455-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7300791-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007161558-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003100072-A1 |
priorityDate | 1989-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 750.