http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006340694-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bd89c0e07c12d4c43d22eb44b082d754 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02 |
| filingDate | 2005-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c740bccd3f91e13d5f869b601ebeaba6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0eaba6557064f7049a41c782d7ff9825 |
| publicationDate | 2006-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2006340694-A |
| titleOfInvention | Protein synthesis by in vitro transcription and translation system using molecular chaperone |
| abstract | PROBLEM TO BE SOLVED: A conventional in vitro transcription / translation system is a whole cell extract like an E. coli extract and originally contains a molecular chaperone. The type and amount of the molecular chaperone according to the protein to be synthesized It was difficult to strictly adjust the conditions. A reconstituted in vitro transcription / translation system consisting only of factors necessary for transcription / translation is used to optimize the type and amount of molecular chaperone to be added. [Selection] Figure 6 |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017532063-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015025865-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3197922-A4 |
| priorityDate | 2005-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 1043.