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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_966a6c1f382ec9bcb5e3839dfd73e5b8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-04
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-707
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2017-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3925fb3d438d863b323647ae7b819ed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31533467ceb5cc1cdc50b62fee0cf5e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_544555338b929665769b4ce89f32da23
publicationDate 2018-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2018007694-A
titleOfInvention Dual probe assay for target nucleic acid detection
abstract The present invention relates to a method for amplifying and detecting a target nucleic acid in a sample, the method performing amplification of the nucleic acid in the sample, and to amplify and detect the target nucleic acid. Provide kits. A target nucleic acid is contacted with an amplification reagent comprising a polymerase, a primer for generating an amplicon, and at least two detectable probes specific for different sequence portions of the amplicon, and the different sequences of the amplicon The presence or absence of the amplicon is detected by detecting hybridization of the above-described probe to the moiety. [Selection figure] None
priorityDate 2012-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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