http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017088750-A1

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filingDate 2016-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57ad9095b8cb5dbb752e943dbe4ca00f
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publicationDate 2017-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2017088750-A1
titleOfInvention Method and kit for deviation amplification of target nucleic acid sequence in sample
abstract Provided is a method for deviation amplification of a target nucleic acid sequence having a mutation relative to a wild type form in a sample, comprising: providing a single-stranded closed sequence complementary to at least a part of a sense strand and/or antisense strand of the wild-type form of the target nucleic acid sequence, wherein one or more locked nucleic acid substitutions are comprised in the closed sequence; providing a PCR reaction system comprising the sample, the closed sequence, and a forward and reverse primer designed according to the target nucleic acid sequence and performing a cyclic amplification reaction, wherein the denaturation steps comprise: raising the temperature to a sufficiently high temperature, contacting the closed sequence with the nucleic acid in the sample, and then cooling to a first temperature to make the closed sequence, the target nucleic acid sequence and the wild-type forming of the target nucleic acid sequence form a duplex, wherein the first temperature is higher than the annealing temperature of the primer and the template, and then raising the temperature to a second temperature of approximately 1-5ÂșC lower than the melting temperature (T m ) of the duplex formed by the closed sequence and the wild type of the target nucleic acid sequence, and higher than the T m of the wild-type form duplex of the target nucleic acid sequence.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107164519-A
priorityDate 2015-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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