http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102876661-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2521-101 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2521-107 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10 |
| filingDate | 2012-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102876661-B |
| titleOfInvention | The amplification detection method of nucleic acid and test kit |
| abstract | The present invention relates to amplification detection method and the test kit of nucleic acid.Particularly, the invention provides a kind of method that nucleic acid contained in sample is increased, wherein, the method comprises: (a) will be used for the primer, polysaccharase and the Nucleotide as nucleic acid amplification substrate that increase to the arbitrary region of this nucleic acid, with the operation of the sample mixed containing this nucleic acid; And the operation that (b) utilizes polymeric enzyme reaction to increase to this region.Wherein, this polysaccharase has the aminoacid sequence that is made up of sequence numbering 1 or the aminoacid sequence with sequence numbering 1 homology, and the amino-acid residue of 651 corresponding to this aminoacid sequence is replaced by L-glutamic acid. |
| priorityDate | 2011-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 60.