http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112680463-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-94 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6844 |
| filingDate | 2021-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-112680463-B |
| titleOfInvention | CP gene of wild pea latent virus and application thereof |
| abstract | The invention discloses a CP gene of a wild pea latent virus, wherein the nucleotide sequence of the CP gene is shown as SEQ ID NO: 1 is shown. The invention also discloses a recombinant vector comprising the CP gene, a specific primer pair for amplifying the CP gene, a primer group for detecting the CP gene of the Vicia victoria latent virus, a kit for detecting the Vicia victoria latent virus and a method for detecting the Vicia victoria latent virus with a non-diagnosis purpose. The detection kit and the detection method thereof do not need a PCR instrument, have low cost and simple operation, can amplify the limited amount of DNA to 100 ten thousand parts with high specificity and high efficiency within 1h, have higher sensitivity than the PCR technology, and have convenient identification of reaction results. |
| priorityDate | 2021-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 147.