http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0257192-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_be3928f66bb2545a8175c61c56146b9a |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-00 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-19 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-16 |
| filingDate | 1988-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81b26df6f8cf8c69463d28ac6b65f164 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13d416a6e8b1994c9021e21f5ecfa8fe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f46f499544416f1c1a1f649562a9c31 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe0ad382b8be749845770d661b03656a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_175756b67eebbce75d0413c6ebd947af http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2940b704f09ea90786053baa40864701 |
| publicationDate | 1990-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H0257192-A |
| titleOfInvention | Production of motilin-like polypeptide, recombinant dna and plasmid for manifestation for producing same polypeptide |
| abstract | PURPOSE: To mass produce motilin by analyzing amino acid structure of motilin as a hormone to manage motion sthenia of digestive tract and smooth muscle contraction of digestive tract and using DNA to code the amino acid structure. n CONSTITUTION: A single stranded DNA to code a peptide containing ≥6 residues of non-charged polar amino acids and methionine at the end, a single stranded DNA to code an amino acid sequence shown by the formula (X is amino acid residue except Met and Asp) and single stranded DNAs containing a base sequence complementary with base sequences of these single stranded DNAs are synthesized, respectively. A duplex DNA is prepared comprising the non- charged amine acid as a leader sequence by using these synthetic single stranded DNAs and specific restriction enzyme recognition sites are added to the ends of the duplex DNA. A plasmid integrated with another protein gene information is cleft with the same restriction enzyme as that of the restriction enzyme recognition site, the preobtained DNA is added to the cleft point to reconstitute a plasmid. A host is transformed with the plasmid. n COPYRIGHT: (C)1990,JPO&Japio |
| priorityDate | 1988-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.