http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103923175-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-07 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-37 |
| filingDate | 2014-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103923175-B |
| titleOfInvention | A kind of fluorogenic substrate for detecting the trypsinase vigor acting on Cry1A class parent toxin and application thereof |
| abstract | The invention discloses a kind of fluorogenic substrate for detecting the trypsinase vigor acting on Cry1A class parent toxin and application thereof.This fluorogenic substrate consists of: fluorescent quenching group-Gly-GLy-Glu-Arg-Ile-Glu-Thr-Gly-Glu-fluorophor.Fluorescent peptide substrates R28 of the present invention is detecting the application in the insect midgut trypsinase vigor directly acting on activation bacillus thuringiesis Cry1A class parent toxin.Compared with traditional proteolytic enzyme detection method, fluorogenic substrate of the present invention has clear and definite specificity and specific aim for detecting the insect midgut trypsinase vigor directly acting on activation bacillus thuringiesis Cry1A class parent toxin, detect the trypsinase vigor only acting on corresponding fluorogenic substrate R28, the strong fluorescent signal produced in enzyme digestion reaction, substantially increases the sensitivity of detection. |
| priorityDate | 2014-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 56.