http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100986960-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2537-164 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6876 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2008-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2010-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2010-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-100986960-B1 |
| titleOfInvention | Analysis of gene methylation and ratio |
| abstract | In the present invention, when a gene is treated with sodium bisulfite in order to confirm methylation of a gene and then PCR is performed as a template, a primer (methylated specific primer) that enables amplification when the gene is methylated, A primer (non-methylated specific primer) that binds to a portion spaced from a portion of a gene to which the primer binds, and which is amplified when the gene is unmethylated, and a primer that is not affected by methylation (common primer) Simultaneously perform PCR using all of the genes so that the PCR product (methylated amplification product) when the gene is methylated according to the degree of methylation of the gene and the PCR product (nonmethylated amplification product) when the gene is unmethylated are different sizes. By amplifying to a method for analyzing the methylation and ratio of the gene.n n n n Methylation, CpG sequence |
| priorityDate | 2008-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 106.