http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010104386-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_430c89d97f6839f5364904e710af9704
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-906
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-723
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filingDate 2010-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82de806180ce2032e4d540c50cddb628
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21d36387597dc6c7363f1168fdbd87d6
publicationDate 2010-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010104386-A
titleOfInvention Sample pretreatment method for measuring glycated amine and method for measuring glycated amine
abstract The present invention provides a sample pretreatment method using glycated amine as a measurement object, and enables measurement of glycated amine with excellent reliability. SOLUTION: After digesting fructosyl amino acid oxidase (FAOD) with a glycated amino acid in a sample, FAOD is further acted on a glycated amine as a measurement target in the sample, and the oxidation-reduction reaction is measured. To measure the amount of saccharified amine. The FAOD that acts on a glycated amino acid and the FAOD that acts on a glycated amine may have the same or different substrate specificities. When the same FAOD is used, the FAOD is allowed to act on the glycated amino acid and decomposed, then the FAOD is deactivated by protease and the glycated amine is decomposed, and the same FAOD is further added to the decomposed product to act. The redox reaction is measured. [Selection] Figure 1
priorityDate 2001-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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