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filingDate 1973-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1975-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b8c133a69020fe6580ff8a2508baf48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e98194de785c6205761358a53d332fb3
publicationDate 1975-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3899397-A
titleOfInvention Glutamic oxalacetic transminase assay method
abstract An improved diazonium coupling procedure for L-aspartate: 2oxoglutarate amino transferase, EC 2.6.1.1, or glutamicoxalacetic transaminase (GOT) assay. The method for determining the glutamic-oxalacetic transaminase in biological fluids involves preparing a substrate of 1-aspartic acid, Alpha ketoglutaric acid, buffer, surfactant and water. The substrate has a pH between about 5 and about 8, preferably 7.5. A sample of biological fluid is admixed with substrate. The admixture is incubated. Then an aprotic solvent is added to the admixture to stop the reaction between the 1-aspartic acid and Alpha ketoglutaric acid which is catalyzed by the glutamic-oxalacetic transaminase. A diazonium dye and methanol is then added to the admixture. The activity level of the glutamic-oxalacetic transaminase by measuring the absorbance against a reagentspecimen blank is determined. The preferred diazonium dye is Diazo Red RC.
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