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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-32
filingDate 1989-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2c5d0686ae2eef3c5056028529c3c34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce8269c3025e8c6663086256d16ee272
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5822925c9f02865a1abc549154fdbacd
publicationDate 1990-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02200200-A
titleOfInvention Determining method of nadh and determination of bile acid using the same method
abstract PURPOSE: To make possible to measure in high accuracy by reacting reduction- type β-nicotinamide adenine dinucleotide(NADH) with oxidation-type glutathione in the presence of specific enzyme. n CONSTITUTION: Oxidation-type glutathione, glutathione.reductase and pH5.5-8 buffer solution containing disulfide-type thiol determining reagent of 5,5'-dithiobis(2-nitrobenzoic acid) are added to a sample containing NADH and reacted at about 37°C for 5-20 min. Next, oxidation-type β-nicotinamide adenine dinucleotide (NAD + ) and reduction-type glutathione are generated in a reacting solution and thiol compound is conjugately generated from the determining reagent. Then, light absorbancy at 300-450nm as characteristic wavelength of the thiol compound is measured to determine NADH. Bile acid is reacted with NAD + in the presence of 3α-hydroxysteroid.dehydrogenase at pH5.5-8, as necessary, and bile acid is determined according to generated amount of NADH. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017534882-A
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priorityDate 1988-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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