http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011188774-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_82cbc291d77c061ac9a216f86ec010a3 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2010-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7ebaedb0704e264f4b344510b5454a7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e5d2ebd1105a02b2200ec3a09a4414a |
publicationDate | 2011-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2011188774-A |
titleOfInvention | High-precision detection method for single nucleotide polymorphism mutations using capillary electrophoresis |
abstract | An inexpensive and simple high-throughput analysis method for the presence or absence of SNP or its mutation is provided that is not affected by the type of target gene. A method for detecting a mutation in a single nucleotide polymorphism or a genotype based on the single nucleotide polymorphism, (1) a gene fragment containing a single nucleotide polymorphism having the same chain length and a wild type gene thereof The target sequence obtained from each fragment and its complementary sequence are separated as single-stranded DNA by simultaneously performing electrophoresis by capillary electrophoresis under strongly acidic conditions, and (2) presence or absence of mutation depending on the number of peaks appearing in the electropherogram Detecting said method. [Selection] Figure 6 |
priorityDate | 2010-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 285.