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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6848
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34
filingDate 2012-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43e44109033537d5b4786832d6febba1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af4f9f3fef279b548d39b521aa61191a
publicationDate 2019-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10273532-B2
titleOfInvention Nucleic acid amplification method
abstract The invention provides an ultra-rapid nucleic acid amplification method performed in a flow channel. Specifically, the invention provides a nucleic acid amplification method for performing a PCR reaction by supplying a PCR sample solution to a nucleic acid amplification device comprising a serpentine channel adapted to perform at least one PCR cycle, the nucleic acid amplification device comprising a DNA denaturation temperature zone corresponding to the curved portions at one side, an annealing temperature zone corresponding to the curved portions at the other side, and an extension temperature zone positioned between the annealing and DNA denaturation temperature zones, wherein the PCR sample solution is introduced in the form of sample plugs separated by gas into the serpentine channel using a pump, the sample solution being supplied into the channel in a state such that the solution is separated by gas into a segment corresponding to one PCR cycle or smaller segments.
priorityDate 2012-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 42.