http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2005090604-A1
Outgoing Links
Predicate | Object |
---|---|
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-542 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-27 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-566 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 |
filingDate | 2005-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2008-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-WO2005090604-A1 |
titleOfInvention | Gene mutation detection method and gene mutation detection kit |
abstract | A solution containing a single-stranded target nucleic acid (10) having a target base (11) related to SNP and the like, and two types of single-stranded detection nucleic acids complementary to a partial sequence sandwiching the target base (11) ( The solution containing 20a) and (20b) is mixed, and the target nucleic acid (10) and the detection nucleic acid (20a) and (20b) are hybridized, thereby intentionally forming a site facing the target base (11). A gap site (21) is constructed. Then, a receptor molecule (30) exhibiting hydrogen bonding and fluorescence is inserted into this gap site (21) which is a hydrophobic field space. Then, the fluorescence intensity change of the receptor molecule (30) based on the difference of the target base (11) is detected, and single base substitution is detected. |
priorityDate | 2004-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 38.