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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2334-10
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34
filingDate 1999-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77ad92ee32e9a4d29e6253bbcd3aa1e0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5cdc33ee1fd7f64310c8775b389464e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5795830e75e3cb973b4183bef773bbe0
publicationDate 1999-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2335613-A1
titleOfInvention Ph-indicator based assay for selective enzymes
abstract Provided herein is a method for the quantitative screening of hydrolase for desired substrate activity using pH indicators which are sensitive to the release of protons from a chemical reaction in a reaction mixture. The method comprises selecting buffer and indicator conditions such that both have the same affinity for portions such that the relative amount of buffer protonated is proportional to the amount of indicator protonated as the pH of the reaction mixture shifts. A reaction mixture is then prepared comprising a buffer, indicator, hydrolase to be tested, and desired substrate to be tested, allowing the hydrolase to react with the substrate. The reaction is monitored by detection of change in color of the reaction mixture, determined by the affect of the reaction on the indicator.
priorityDate 1998-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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