http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2007046158-A1
Outgoing Links
Predicate | Object |
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classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6839 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6816 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2006-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2009-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-WO2007046158-A1 |
titleOfInvention | Nucleic acid analysis method |
abstract | The present invention enables stable amplification of a small amount of nucleic acid and highly sensitive analysis by improving the efficiency of hybridization between a primer or probe and a sample. That is, the present invention provides a first sequence complementary to one strand of a double-stranded nucleic acid, a second sequence complementary to the other strand, and a third sequence linking the first sequence and the second sequence. And a step of hybridizing at least one kind of the first probe to the double-stranded nucleic acid and a step of hybridizing at least one type of the second probe to the double-stranded nucleic acid. The present invention relates to a nucleic acid analysis method. |
priorityDate | 2005-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 219.