http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105886501-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-682
filingDate 2016-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105886501-B
titleOfInvention Nucleic acid signal amplification sequence and amplification method
abstract The present invention relates to molecular biology fields, and in particular to a kind of nucleic acid signal amplification sequence and nucleic acid signal amplification method.Nucleic acid signal amplification sequence of the present invention includes the repetitive sequence composition of a leader sequence and a several multiples, and the leader sequence is complementary with purpose target sequence, and the repetitive sequence is complementary with reporter probe sequence.Nucleic acid signal amplification sequence of the present invention, which can be captured purpose target by leader sequence, to be hybridized, and combines corresponding reporter probe that signal amplification can be realized using the repetitive sequence of several multiples, to detect the nucleic acid signal of purpose target.Enzyme is needed relative to round pcr to maintain hybridization system, and the detection that nucleic acid substances are realized under the premise of not increasing detectable substance concentration may be implemented in the present invention, and stability is good, and repeatability is high, and at low cost, testing process is short.
priorityDate 2016-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 33.