http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108977505-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6834 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6841 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6834 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6841 |
| filingDate | 2018-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-108977505-B |
| titleOfInvention | Method for rapidly screening microbial strains generating tetrodotoxin and digoxin labeled DNA probe used by same |
| abstract | The invention relates to the technical field of marine organisms, in particular to a method for rapidly screening microbial strains generating tetrodotoxin and a digoxin labeled DNA probe used by the same. Through colony in-situ spot molecular hybridization, the probe can specifically detect whether tetrodotoxin synthesized sxt gene nucleic acid exists in a bacterial strain DNA sample to be detected, and a toxin-producing positive bacterial strain is screened. The method utilizes the in-situ extract of the strain DNA to carry out colony spot hybridization, and can complete 96 samples for screening within 8-10 hours. The method is rapid, strong in specificity and high in accuracy. |
| priorityDate | 2018-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 107.