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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-495
filingDate 1994-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7614f4abe856fd92129c70bfda95a00c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a8b68f88c6e772a451355eadabf978c
publicationDate 2007-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2153789-C
titleOfInvention Biologically active tgf-.beta.1 and tgf-.beta.2 peptides
abstract The invention relates to peptides corresponding to regions of the amino acid sequence of TGF-.beta.1 or TGF-.beta.2 which retain, either in monomeric or polymeric forms, at least some of the biological activity of the respective full length TGF-.beta.. The monomeric form of the peptide derived from TGF-.beta.1 comprises the following amino acid sequence: CVRQLYIDFRKDLGWKWIHEPKGYHANFCLGP. The monomeric form of the peptide derived from TGF-.beta.2 comprises the following amino acid sequence: CLRPLYIDFKRDLGWKWIHEPKGYNANFCAGA. Dimers may be formed via disulfide bonds between the amino-terminal cysteine residues, the carboxy-terminal cysteine residues, or amino- and carboxy-terminal cysteine residues of the monomer subunits.
priorityDate 1993-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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