http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100911516-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P19-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P21-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12M1-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00 |
| filingDate | 2004-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2009-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100911516-B1 |
| titleOfInvention | High throughput synthesis method and synthesizing apparatus for automatically performing the method |
| abstract | Development of system technology for high-throughput in vitro synthesis reaction methods of biopolymers such as proteins and RNA. Specifically, a synthesis system using a template material as a raw material, the cell-free synthesis method and an automatic synthesizer using the method comprising the following means, control means, or a combination thereof; 1) The template material, the substrate, and the reaction solution are contacted to lead to the synthetic reaction system. 2) The solution is diluted with the reaction system outside the synthesis reaction system before or after the synthesis rate decreases or before or after the synthesis reaction is stopped. 3) The dilution treatment is followed by the concentration treatment. 4) Return the reaction system to the synthetic reaction system. Or, 1) contact the template material, the substrate, and the reaction solution to lead to a synthetic reaction. 2) The solution is concentrated by leaving the reaction system outside the synthesis reaction system before or after the synthesis rate decreases, before or after stopping the synthesis reaction, or during these processes. 3) Concentration treatment is followed by dilution treatment. 4) Return the diluted reaction system to the synthetic reaction system.n n n n High throughput, synthesis method, synthesis apparatus, cell-free system, in vitro synthesis reaction |
| priorityDate | 2003-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 177.