http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005160430-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_338209e62a2b0c980ba7c67789c011af |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
filingDate | 2003-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca2ebbdee0394579c44ba62d20bb8f53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60063f36f35e1fe27047da0c8f22c971 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c460d639834c1c1b0789546644e0968 |
publicationDate | 2005-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2005160430-A |
titleOfInvention | Gene sequence inspection method |
abstract | 【Task】 An object of the present invention is to provide a method that can easily and accurately test a large number of specimens with a simple and accurate inspection of a base sequence, in particular, insertion and deletion of a repetitive sequence of a specific base in a SNP and a promoter region. . [Solution] It has a base complementary to the specific base to be examined in the test nucleic acid sample at the 3 ′ end, and the second base from the 3 ′ end is complementary to the base of the test nucleic acid, and is upstream from the third. A primer obtained by substituting at least one base species of the above with a base species different from a base complementary to the test nucleic acid base (hereinafter, this primer is defined as a detection primer) is hybridized to the test nucleic acid sample, and the substrate When a primer extension reaction is carried out with a polymerase and it is detected whether or not the primer extension reaction occurs corresponding to a specific base sequence, a binding pair capable of specifically binding the product of the primer extension reaction to the product, Provided is a base sequence or mutation test method that can easily and accurately test a large number of specimens by introducing and detecting a binding method. [Selection] [Figure 2] |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20180131581-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2017170644-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11702688-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017170644-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20200031615-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019022132-A1 |
priorityDate | 2003-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 115.