http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105886605-B

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6869
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883
filingDate 2015-03-05^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-07-30^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-07-30^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105886605-B
titleOfInvention The amplimer and detection method of PKD2 detection in Gene Mutation
abstract The invention belongs to medicine vitro diagnostic techniques, and in particular to the amplimer and detection method of autosomal dominant polycystic kidney disease Disease-causing gene PKD2 abrupt climatic change.The amplimer designs 4 pairs of PCR primers using the sequence information of PKD2 gene, carries out targeting amplification to PKD2 by long-chain PCR, amplification region includes whole exons and most of intron sequences and 5 ' non-translational region sequence of part and 3 ' non-translational region sequences.Long-chain PCR targeting amplification is combined the next-generation sequencing technologies of latest development by the method, is simplified targeting sequencing process, is improved the detection range and flux of PKD2 gene mutation, shorten detection cycle, reduce costs.
priorityDate 2015-03-05^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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