http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103014156-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e8bc7ad34a077841f46dd13439a9956d http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e3749e4d9f14e99adc82a7af38d2ce70 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-01 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2012-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2014-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b88a7d4a468f5662b0d1162eeb2e1af8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e301e7de404b04074f7fd9f64625ccef http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4e761db9259d33fbb2853e0b884e832 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b99413609e66d212d556348d2cae8836 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaab05bdff01dbdf90bc6db734dd90fa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f78275b96f3d7a88252aad87ff51eca http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ec74dc5d036704019de71b075351bd5 |
| publicationDate | 2014-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103014156-B |
| titleOfInvention | Loop mediated isothermal amplification detection primer group, detection method and kit for enterococcus faecalis |
| abstract | The invention discloses a loop mediated isothermal amplification detection primer group, a detection method and a kit for enterococcus faecalis. The detection primer group is as follows: an upstream outer primer is F3:5'-GCCATTCCTCATGGAACAG-3'; a downstream outer primer is B 3:5'-CCACGTTATCCATATCACTACA-3'; an upstream inner primer is FIP:5'-CGGTGCCAAAATTAACACCCTTTAGTGAAAAAATCAGGAATCTGTG-3'; a downstream inner primer is BIP:5'-TGCTACCGTATTATTTGGGATTGCAAAGTGCAATTTGTTGGACTA-3'. The detection method has the advantages of high flexibility, strong specificity, high accuracy, short detection time. From sample treatment to report only takes 12 hours, a PCR (polymerase chain reaction) and an electrophoresis apparatus do not need, the operation process is simple, compared with other PCR technology, the detection method has higher specificity, is applicable to self-detection of basic level detection organizations and drinking water processors. |
| priorityDate | 2012-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 191.