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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34
filingDate 1993-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a150cf72bed945ba096feb8772d21386
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cf2d2a8f51fe0e1a7e7987da818f48d
publicationDate 1994-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06205699-A
titleOfInvention Method for measuring α-amylase activity and reagent for measuring α-amylase activity
abstract (57) [Summary] [Objective] To provide an α-amylase activity measuring method capable of accurately and simply measuring the true activity of α-amylase using an automatic analyzer, and a reagent for use in this measuring method. To do. [Structure] A substrate containing a maltooligosaccharide whose reducing end is modified with a dye and a sample containing α-amylase in the coexistence of calcium ions are used to optimize the activity of α-amylase. The first step of degrading the substrate by acting with H, α-glucosidase and calcium ion scavenger to the product obtained in the first step, the second step of acting at the activity optimum pH of α-glucosidase, and An α-amylase activity measuring method comprising a third step of colorimetrically quantifying the dye produced in the two steps. A first solution containing a substrate consisting of a dye-modified maltooligosaccharide, a water-soluble calcium salt compound and a buffer solution having an activity optimum pH of α-amylase, and α-glucosidase, Reagent for measuring α-amylase activity comprising a second liquid containing a calcium ion capturing agent and a buffer solution
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013068642-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006136882-A
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