http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111944889-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 |
| filingDate | 2020-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-111944889-B |
| titleOfInvention | PCR amplification composition for detecting chromosome aneuploid number abnormality and detection kit |
| abstract | The invention relates to a PCR amplification composition and a detection kit for detecting chromosome aneuploid number abnormality, wherein the composition can simultaneously carry out composite amplification on 19 STR loci on 16 and 22 chromosomes; the invention discloses a detection kit for human chromosome number abnormality, and particularly relates to an automatic, high-throughput and low-cost rapid detection kit which is suitable for STR gene analysis of Chinese population and is developed by applying quantitative fluorescence PCR (polymerase chain reaction) and capillary electrophoresis technology aiming at chromosomes with common number abnormality, namely 16 and 22, for prenatal diagnosis and spontaneous abortion analysis. |
| priorityDate | 2020-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 28.