http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104357583-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6851 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-70 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70 |
| filingDate | 2014-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104357583-B |
| titleOfInvention | The real-time fluorescent RT-PCR detection reagent box of Ba Maha forest virus and method |
| abstract | The invention discloses real-time fluorescence RT PCR kit and the method for detection Ba Maha forest virus, the real-time fluorescence RT PCR kit of detection Ba Maha forest virus includes 2 × RT PCR Buffer, 25 × RT PCRenzymeMix, upstream and downstream primer, the nucleotide sequence of probe, the primer and probe is as shown in SEQ ID No.1, SEQ ID No.2 and SEQ ID No.3；Negative control, positive control.The real-time fluorescence quantitative PCR detection kit that the present invention provides is easy to use, and the reagent used by kit is few, enormously simplify operating process, decreases the pollution in operating process, detects high specificity, highly sensitive, it is adaptable to quick detection Ba Maha forest virus. |
| priorityDate | 2014-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.