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乳酸脱氢酶及其同工酶-1活性的生物发光测定。

Bioluminescent assay of lactate dehydrogenase and its isoenzyme-1 activity.

作者信息

Pråhl M S, Karp M T, Lövgren T N

出版信息

J Appl Biochem. 1984 Oct-Dec;6(5-6):325-35.

PMID:6536646
Abstract

A bioluminescent assay based on the bacterial luciferase reaction has been developed for the determination of total lactate dehydrogenase and heart-specific lactate dehydrogenase isoenzyme-1 activity in serum. The lactate dehydrogenase-catalyzed reaction was measured in both directions, but NADH formation (lactate----pyruvate) is recommended because it allows the use of optimal reaction conditions. Internal calibration with a known amount of NADH accounts for possible interference from samples when both NADH formation and consumption are followed. The bioluminescent method is sensitive, has good precision, and is readily automated. Serum lactate dehydrogenase isoenzyme-1 was immunochemically isolated and the activity was assayed by bioluminescence. A good correlation between the bioluminescent assays and the conventional spectrophotometric procedure used as reference was obtained.

摘要

已开发出一种基于细菌荧光素酶反应的生物发光测定法,用于测定血清中总乳酸脱氢酶和心脏特异性乳酸脱氢酶同工酶-1的活性。乳酸脱氢酶催化的反应在两个方向上进行测定,但推荐测定NADH的形成(乳酸→丙酮酸),因为这样可以使用最佳反应条件。当同时监测NADH的形成和消耗时,用已知量的NADH进行内部校准可消除样品可能产生的干扰。该生物发光方法灵敏、精密度好且易于自动化。血清乳酸脱氢酶同工酶-1经免疫化学分离,其活性通过生物发光法测定。生物发光测定法与用作参考的传统分光光度法之间具有良好的相关性。

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