http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20150038944-A

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-154
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6876
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
filingDate 2013-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2015-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20150038944-A
titleOfInvention Method for Analysis of Gene Methylation and Ratio Thereof
abstract In order to confirm the methylation of a gene, the present invention is characterized in that a DNA containing a specific gene is treated with sodium bisulfite, followed by ligating and amplifying oligonucleotides using the DNA as a template, , Oligonucleotides enabling the linkage when the specific gene is unmethylated, and oligonucleotides capable of linking when the specific gene is unmethylated and a nucleotide sequence complementary to the nucleotide sequence complementary to the 3 ' end of the oligonucleotide An oligonucleotide that makes complementary binding is used for the linking reaction and the amplification reaction to form an amplification product when the specific gene is methylated and an amplification product when the specific gene is unmethylated according to the degree of methylation of the specific gene These amplification products are the same with the same capture probe Securely by generating a different signal to the complementary bonding to a method for analyzing the methylation status and rate of the gene.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11603555-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20190105224-A
priorityDate 2013-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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