http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101522836-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-124 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6869 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6853 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-11 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2013-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-101522836-B1 |
| titleOfInvention | New primer and genotyping method of sla-dqa using genomic pcr based direct sequencing |
| abstract | The present invention relates to a method for analyzing an SLA-DQA genotype, and more particularly, to a method for analyzing an SLA-DQA genotype through direct sequencing of genomic DNA. According to the present invention, a primer set suitable for genomic PCR and amplifying all the alleles and minimizing the allelic variation in amplification efficiency is designed, whereby allelic information and genomic DNA can be obtained without cloning step PCR and direct sequencing can be used to accurately and easily analyze the genotype of all SLA-DQA alleles. |
| priorityDate | 2013-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 82.