Alkaline reagent solution for eliminating ammonia in an assay

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving oxidoreductase

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435 25, 435189, 435190, 435822, 435966, C12Q 126, C12Q 132, C12N 902, C12N 904

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active

058719482

ABSTRACT:
The invention relates to an ammonia elimination reagent for use in an enzymatic assay of a biological substance which produces ammonia as the reaction product. The reagent is an alkaline solution of pH 9 to 11 and contains Sulfolobus-derived thermostable isocitrate dehydrogenase, 2-oxoglutaric acid, a reducing coenzyme, isocitric acid, glutamate dehydrogenase, and a divalent metal salt. The reagent can be stored in solution and has excellent stability under conditions of alkaline pHs.

REFERENCES:
patent: 4742001 (1988-05-01), Marui et al.
patent: 5258286 (1993-11-01), Marui et al.
patent: 5336608 (1994-08-01), Niimura et al.
Danson, M.J. and Wood, P.A. Isocitrate dehydrogenase of the thermoacidophilic archaebacterium Sulpholobus acidocaldarius, FEBS Lett., 172:289-293, 1984.
Fujita, T., Takata, S. and Sunagara, Y. Enzymatic rate assay of creatinine in serum and urine, Clin. Chem. 39:2130-2136, 1993.
Abstract of Japan, JP-A-02 255 098, Oct. 15, 1990.
Abstract of Japan, JP-A-63 214 182 Sep. 6, 1988.
Fossati et al, "A step forward in enazymatic measurement of creatinine", Clinical Chemistry, vol. 40, No. 1 1994, pp. 130-137.
Chemical Abstracts (1984) 100:188433d cited in the examination of USSN 06/878561 which is the original USSN of US Patent No. 5,258,286.

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