http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0594164-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f97f0fa258a008bf056ad04b7f380dda |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-81 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T436-255 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-128 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6821 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-37 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-37 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68 |
| filingDate | 1993-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26777a10b8d51650709d6454ae99cd8d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_393b75423b715696fcf34ffa91b013c5 |
| publicationDate | 1994-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0594164-A1 |
| titleOfInvention | Method for peptide C-terminal fragment sequence analysis and apparatus for collecting peptide fragment |
| abstract | The present invention relates to a method for peptide C-terminal fragment sequence analysis, in which the fragment collection is carried out on an allylamine group-derivatized polymer membrane or on allylamine group-derivatized glass fiber filter paper; the collected C-terminal fragment is immobilized theron using a water-soluble carbodiimide etc.; and the obtained immobilized product is subjected directly to amino acid sequence analysis. The present invention also relates to an apparatus for collecting a peptide fragment. According to the method of the present invention, peptides which are rich in hydrophobic groups in their C-terminus and are therefore difficult to trap with polyvalent ion carriers, currently used in the gas-phase sequencer, can be completely analyzed up to their C-terminus. Also, amino acid sequence analysis can be made even when the amount of C-terminal fragments is very small. In addition, since collection and immobilization of fragments can be done in the same bottle, the risks of contamination and mechanical loss are very low. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6156527-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1265072-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-721390-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7163803-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02099436-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106855477-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02099436-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9832876-A1 |
| priorityDate | 1992-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.