http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011188774-A

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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

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