http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010207160-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9bceffddb90b9b3da8a772212961764b |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2009-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a065adc2e3ddb81361f06dcfb7492ddc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9dd93b59205e75f5e701dadbc33d2ef1 |
| publicationDate | 2010-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2010207160-A |
| titleOfInvention | Enzyme reagent for DNA 3 'terminal modification removal |
| abstract | The present invention provides a new use of an unknown function of a heat-resistant DNA polymerase, or a method for using the same. The DNA has a function of cleaving deoxyribose-3′-phosphate ester at the 3 ′ end, and the cleaving function is specific to the substrate regardless of the type of substituent that binds to the phosphate group of the ester. A method for performing PCR gene amplification, real-time PCR, or repairing or amplifying damaged genes of ancient organisms using a primer that also serves as a probe, utilizing the activity of DNA polymerase, which has low properties. [Selection figure] None |
| priorityDate | 2009-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 221.