http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2364833-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac316c4307d2a84add2bae0328f607bd |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-702 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-701 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70 |
filingDate | 2010-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff67acc1bd5c837589ab586bc794be6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_529187f3420c157af426b1b5acc976fa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dbd7f92f698ce7a18a4efdd03d43aeb |
publicationDate | 2011-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-2364833-A1 |
titleOfInvention | VIRUS WEST NILE GENOMIC AMPLIFICATION METHOD. |
abstract | West genomic genomic amplification methodnNile The method is based on the amplification of an area of the regionn3 'non-coding virus, preferably by Time PCRnReal, thanks to the use of a pair of primers minimallyndegenerates, allowing West Nile virus amplificationnpresent in a sample of any of the known lineages. Henamplified fragment is preferably detected with a probenspecific to the area, also minimally degenerated. The couple ofnDegenerate primers chosen, as well as the preferred probe, givenleading to high sensitivity in the detection of all lineages andnalso at a high specificity for West Nile virus. |
priorityDate | 2010-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 126.