乳酸脱氢酶及其同工酶-1活性的生物荧光测定。

Journal of applied biochemistry Pub Date : 1984-10-01
M S Pråhl, M T Karp, T N Lövgren
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引用次数: 0

摘要

建立了一种基于细菌荧光素酶反应的生物荧光法,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都被测量,但NADH的形成(乳酸----丙酮酸)是推荐的,因为它允许使用最佳的反应条件。内部校准与已知数量的NADH说明可能的干扰,当NADH形成和消耗后,样品。该方法灵敏度高,精密度好,易于自动化。采用免疫化学方法分离血清乳酸脱氢酶同工酶-1,并用生物发光法测定活性。生物发光测定法与常规分光光度法具有良好的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioluminescent assay of lactate dehydrogenase and its isoenzyme-1 activity.

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.

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