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METHOD OF DETERMINING PEROXIDASE ACTIVITY AND SUBSTRATE MIXTURE FOR DETERMINATION OF PEROXIADSE ACTIVITY

机译:测定过氧化物酶活性和底物混合物的测定过氧化物酶活性的方法

摘要

FIELD: chemistry.;SUBSTANCE: group of inventions relates to biotechnology and can be applied in creation of analytic methods with application of peroxidases. Method includes preparation of substrate mixture, introduction of peroxidases in substrate mixture with the following registration of intensity of formed luminescence. Substrate mixture includes the following components, given in final concentrations: buffer solution 10-125 mM, luminol 0.05-8 mM, hydrogen peroxide 0.05-8 mM, 4-aminopyridines 0.1-10 mM, N-carboxyphenothiazine, or N-(carboxymethyl)phenothiazine, or N-(2-carboxyethyl)phenothiazine 0.1-10 mM. And pH of buffer solution constitutes 7.9-9.0.;EFFECT: invention ensures obtaining of high intensity of chemiluminescence and, accordingly, high sensitivity of peroxidase activity determination.;4 cl, 8 ex
机译:发明领域本发明涉及生物技术,并且可以通过应用过氧化物酶而用于创建分析方法。方法包括制备底物混合物,将过氧化物酶引入底物混合物中,随后记录形成的发光强度。底物混合物包括以下成分,以最终浓度给出:缓冲溶液10-125 mM,鲁米诺0.05-8 mM,过氧化氢0.05-8 mM,4-氨基吡啶0.1-10 mM,N-羧基吩噻嗪或N-(羧甲基)吩噻嗪或N-(2-羧乙基)吩噻嗪0.1-10 mM。缓冲溶液的pH值在7.9-9.0之间。

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