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filingDate 2017-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d481a23839c94519a618be3cd9179247
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publicationDate 2017-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2017140042-A
titleOfInvention Methods and compositions for rapid multiplex amplification of STR loci
abstract The present invention relates to a method for multiplex polymerase chain reaction (PCR) amplification of a short tandem repeat (STR) locus that can be used to rapidly generate a highly specific STR profile from a target nucleic acid. A method for detecting the presence of a single nucleotide polymorphism (SNP) of a nucleic acid in a sample containing nucleic acid, wherein hybridization between eight or more unlabeled oligonucleotides in the sample and the nucleic acid is possible The sample and oligonucleotide in contact with each other in solution to generate primer extension products, each in the presence of multiple dideoxyNTPs each labeled with one of eight or more different fluorescent dyes. The primer extension is labeled with a fluorescent dye by a laser-excited fluorescence method using a step-steer mode galvanometer and a spectroscope to detect the fluorescence from each fluorescent dye by primer extension reaction. A method of detecting a SNP by detecting a product. [Selection figure] None
priorityDate 2011-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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