http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2007010950-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2400-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-37 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-26 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-37 |
| filingDate | 2006-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-WO2007010950-A1 |
| titleOfInvention | Method and kit for measuring glycated protein |
| abstract | In the present invention, a protease is allowed to act on whole blood and / or a blood cell sample, and then an erasing reagent containing one or more ketoamine oxidases is allowed to act to produce α-glycated amino acid, ε-glycated amino acid, and ε-glycated. The present invention relates to a method for measuring α-glycated peptide in the sample using oxidase acting on α-glycated peptide after erasing the peptide or a combination thereof, and an erasing reagent and kit therefor. According to the present invention, it is possible to reduce a measurement error in measurement of a glycated protein such as glycated hemoglobin and obtain an accurate measurement value. |
| priorityDate | 2005-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 264.