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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_601d76f2c8c69d66f52461892ec3308a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-66
filingDate 1996-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5195dbf2b88269b34c5a0cfea57c6f51
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_021c2351c6943c937d2816129a2ebc32
publicationDate 1998-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10165200-A
titleOfInvention Method for measuring microbial ATP
abstract PROBLEM TO BE SOLVED: To provide a method for measuring a microorganism ATP, which can efficiently, accurately, and in a short time measure a microorganism in a sample containing a large amount of free ATP. SOLUTION: An ATP decomposing reagent is added to a sample (sample) containing a large amount of free ATP not derived from a microorganism to decompose free ATP in the sample, and then an ATP extraction reagent is added to the sample in which free ATP has been decomposed. ATP is added to extract ATP from the microorganism. At this time, the ATP extraction reagent simultaneously inactivates the ATP degradation reagent previously added to the sample, and then brings the sample into contact with a luminescent reagent containing an enzyme reaction inhibition inhibitor, Light generated by the biochemiluminescence reaction is measured by a biochemiluminescence measuring device.
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type http://data.epo.org/linked-data/def/patent/Publication

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