http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103882153-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9d6bf88871e8b4ef559885037fde9545 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-70 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-93 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70 |
| filingDate | 2014-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5b30d9a9dbaef89ce3408d8c106a636 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6dbd1663cc704b1d84996599cdc22f56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_563cc5c43f3f7b5434b295c458766988 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c0a243777e87e025174f0d161b01e7e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_258761396cf615431eafa13176328fe0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8622d3e9f8bdfc9b6960b398a94abe0d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e3851136357a046c6147e97abfd05c0 |
| publicationDate | 2015-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103882153-B |
| titleOfInvention | Fluorescent quantitative primer group for visual differential diagnosis of waterfowl parvoviruses |
| abstract | The invention discloses a real-time fluorescent quantitative PCR (Polymerase Chain Reaction) primer group for visual detection on infection conditions of goose parvovirus (GPV) and muscovy duck parvovirus (MDPV) and a method thereof. According to the method, the detection on the infection conditions of GPV and MDPV is carried out by using dissolution curve temperature difference caused by the difference between nucleotide GC contents of GPV and MDPV specific gene fragment regions amplified by primers, and the infection conditions of GPV and MDPV can be subjected to visual differential diagnosis specifically by only combining the SYBR Green I based real-time fluorescent quantitative PCR primer group to dissolution curves which are automatically generated after reaction is ended. The method disclosed by the invention is simple and is relatively high in efficiency and accuracy. |
| priorityDate | 2014-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.