http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S56144098-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_875ecb1d71f9569767de393adb6bc821
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-66
filingDate 1980-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dab90d2483594ac766e0a503b55b9b0e
publicationDate 1981-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S56144098-A
titleOfInvention Measurement of enzyme or substrate by luminescence of organism
abstract PURPOSE: To measure an enzyme or substrate qualitatively or quantitatively, by adding an enzyme, substrate, or coenzyme to a test sample to cause an enzyme reaction, introducing finally the reaction to a reaction process wherein ATP (adenosine triphosphate) is formed or consumed, adding luciferin and luciferase to the reaction, followed by measuring an amount of luminescence caused by an organism. n CONSTITUTION: In the case where an amount of triglyceride is measured, when it is reacted with an enzyme hydrolyzing glycerol ester, it is decomposed into glycerol and a fatty acid. ATP and an enzyme rearranging phosphoric acid group are added to the prepared glycerol, to give glycerol-3-phosphate and adenosine diphosphate. An amount of excess ATP is subjected to luminescence by an organism with luciferin and luciferase, and the luminescence is measured. n COPYRIGHT: (C)1981,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4902190-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7909563-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8403618-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6672823-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7008167-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63233799-A
priorityDate 1980-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 20.