http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019228542-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e5bd1a176ef2d8d39b992712a7df6743
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6848
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6848
filingDate 2019-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a14c964b28ea9ca0727975f79a2db2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c2c969a91a2f43d743cb9b563eee35a
publicationDate 2019-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2019228542-A1
titleOfInvention Primer 5' end reverse complementary fluorescent pcr and test kit
abstract Disclosed is a primer 5' end reverse complementary fluorescent PCR, wherein a primer 5' end pair is added to a sequence for reverse complementary fluorescent PCR amplification, amplification product ends are complementary, and target product 3' ends may also be mutual templates and mutual primers to increase amplification efficiency. The sensitivity is increased by 50 times on the basis of a conventional PCR index amplification of 109-12, or 5 fewer amplification cycles are performed under same sensitivity conditions. In addition, the primer 5' end complementarity does not extend but rather inhibits original primer pair 3' end polymerisation non-specificity, or the 5 fewer amplification cycles avoid primer non-specific amplification regions. An amplification product of primers having central portion same sequences and 3' final 1-2 base adenine ends + UDG enzymolysis with dU instead of dT in combination with mineral oil sealing causes no primer dimer (PD) production within PCR reaction cycles and prevents product aerosol cross-contamination.
priorityDate 2018-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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