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采用薄层琼脂糖荧光技术测定乳酸脱氢酶同工酶的准确性如何?

How accurate are lactate dehydrogenase isoenzyme estimations by the thin-layer agarose fluorescent technique?

作者信息

McKenzie D, Clark P I, Henderson A R

出版信息

Clin Chem. 1976 Dec;22(12):1995-8.

PMID:1000797
Abstract

We offer an assessment of the accuracy of the thin-layer agarose fluorescent technique of Elevitch et al. [Am. J. Clin. Pathol. 46, 692 (1966)]. We used semi-purified human lactate dehydrogenase isoenzymes 1 and 5. Both the lactate lead to pyruvate and pyruvate lead to lactate assays [Clin. Chem. 20, 1462 (1974)] appear to give, within the errors of the techniques used, a substantially unbiased estimate of both LD-1 and LD-5, although this must remain a provisional conclusion until a definitive method of assay for the total and isoenzymic LD activities is created. Introducing a buffer into the substrate mixture (lactate lead to pyruvate assay) had no effect on these findings except at extremes of pH, when marked inaccuracies occurred.

摘要

我们对埃莱维奇等人[《美国临床病理学杂志》46, 692 (1966)]的薄层琼脂糖荧光技术的准确性进行了评估。我们使用了半纯化的人乳酸脱氢酶同工酶1和5。乳酸转化为丙酮酸以及丙酮酸转化为乳酸的测定方法[《临床化学》20, 1462 (1974)],在所使用技术的误差范围内,似乎对LD - 1和LD - 5都给出了基本无偏差的估计,不过在建立总LD活性和同工酶LD活性的确切测定方法之前,这仍只能是一个初步结论。在底物混合物(乳酸转化为丙酮酸的测定)中引入缓冲液,除了在极端pH值时会出现明显不准确的情况外,对这些结果没有影响。

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