http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105441595-B

Outgoing Links

Predicate Object
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-166
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-707
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6851
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-706
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6851
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70
filingDate 2016-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105441595-B
titleOfInvention It is a kind of for detecting the digital pcr absolute quantitation parting detecting reagent of HBV-B/C
abstract The present invention discloses a kind of for detecting the digital pcr absolute quantitation parting detecting reagent and its detection method of HBV-B/C;The kit includes DNA extracting solution, digital pcr reaction buffer A, digital pcr reaction buffer B, HBV-B viral gene positive quality control, HBV-C viral gene positive quality control, negative Quality Control and inner mark solution;Method includes the following steps:1)By inspection sample treatment;2)The processing of quality-control product;3)Prepare digital pcr reaction mixture;4)Micro- reaction drop is generated, and carries out digital pcr reaction amplification;5)Fluorescence signal is read, HBV type is analyzed and calculates respective copy number.The present invention uses digital pcr technology and Two Colour Fluorescence probe, while detecting two hypotypes of HBV, and independent of external reference substance and standard curve, easy to operate, can be directly to the accurate absolute quantitation of HBV.
priorityDate 2016-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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