http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017178587-A9
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9f422ac028a4af49898a3d32e38e2008 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f63ec271feb191a4c0f391dd11702762 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a4e7069148df052d69567e31b142ae98 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1271c5dc0f9289574052f5fa187c0fc7 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-689 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2017-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb38b04ebaabd18d5d53f502afe0b687 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abd0e0c32b29d5921f85610523c8e97d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4e5b8b619c2104eeb242ba60de01308 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f756cb48f848953a0e16dee459d31332 |
| publicationDate | 2018-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-2017178587-A9 |
| titleOfInvention | Method for universal detection and quantification of mycoplasma (mollicutes) 16s rdna by quantitative polymerase chain reaction amplifying a 1.5 kilobase fragment |
| abstract | The present invention relates to a method for detecting mycoplasma 16S rDNA 1.5 kilobase fragment amplified by quantitative PCR. One of the most critical limitation of the qPCR is the DNA fragment length to amplify. The existing qPCR methods does not permit the amplification of long DNA fragments. Here the inventors demonstrate for the first time the amplification of mycoplasma 16S rDNA 1.5 kilobase fragment using qPCR based on real- time polymerase chain reaction. In particular, the present invention relates to a method for universal detection and quantification of mycoplasma 16S rDNA 1.5 kilobase fragment in a sample comprising contacting said sample with degenerate primers amplified by quantitative PCR or qPCR and using a DNA loading probe. |
| priorityDate | 2016-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 111.