http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008516242-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T436-25875 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T436-24 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6818 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6848 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01J49-02 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N27-62 |
| filingDate | 2005-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2008-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2008516242-A |
| titleOfInvention | Simultaneous sequence analysis of amino and carboxyl termini |
| abstract | The present invention relates to novel methods for identifying polypeptides by deriving carboxyl and amino terminal amino acid sequences by mass spectrometry. The method involves dissociating a highly charged peptide precursor ion (eg, z> 4) with an electron transfer dissociation-induced anion, then removing these reagents to produce a second proton transfer-induced cation type. The process of introducing. A series of sequences that can be easily interpreted to convert the ETD product primarily into the +1 charge state to reduce highly charged c and z-type fragments and reveal the amino and carboxyl terminal sequences, respectively. The second PTR reaction duration is adjusted to produce an m / z spectrum containing c and z-type fragment ions. [Selection] Figure 5 |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013504758-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010522957-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8927295-B2 |
| priorityDate | 2004-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 169.