http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105759045-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-577 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-535 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-535 |
| filingDate | 2016-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2017-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105759045-B |
| titleOfInvention | One kind is directed to aflatoxin B1Detection method |
| abstract | The invention provides one kind to be directed to aflatoxin B 1 Detection method, this method is based on direct competive ELISA technology, after first monoclonal antibody is coated with, add testing sample and catalase C100 mark aflatoxin B 1 , the aflatoxin B in sample 1 With the aflatoxin B of catalase mark 1 It is emulative to be combined with monoclonal antibody fixed on ELISA Plate, decomposing hydrogen dioxide solution is catalyzed by catalase, the fluorescent quenching of the cadmium telluride quantum dot to mercaptopropionic acid modification is reduced, according to fluorescence intensity come aflatoxin B in judgement sample 1 Content.Novelty of the invention introduces new catalase, and reaction precision is improved while cost is reduced；At the same time, present invention uses the cadmium telluride quantum dot of more sensitive novel fluorescence substrate mercaptopropionic acid modification, the luminous sensitivity of more traditional tmb substrate to be obviously improved. |
| priorityDate | 2016-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 200.