http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009240312-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_995094f5776a302a2dda5d52f5dc1c79 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6844 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6816 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6816 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6844 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 |
| filingDate | 2009-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae19c27955b673c6a14c68a9bdbeddd5 |
| publicationDate | 2009-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2009240312-A |
| titleOfInvention | Rolling circle replication of padlock probe |
| abstract | Various methods are used to detect single or multiple nucleotide variations. Many methods rely on amplifying the target sequence, generally by PCR, prior to analysis. Therefore, significant information regarding the location of allelic variation is lost. Providing detection methods that compensate for this shortcoming. A target nucleic acid is cleaved near or preferably at a site that hybridizes with a lock probe, and the 3 ′ end of the cut target nucleic acid is a primer for replicating the rolling circle of the lock probe. Including functioning as Also included is a method of assaying a polyepitope target by utilizing two affinity probes, each with an oligonucleotide label, and a locking probe for rolling circle replication coupled to two affinity probes. [Selection figure] None |
| priorityDate | 1998-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.