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N-乙酰谷氨酸合成酶:人肝脏中的酶活性测定

N-Acetylglutamate synthetase: enzyme assay in human liver.

作者信息

Colombo J P, Krähenbühl S, Backmann C, Aeberhard P

出版信息

J Clin Chem Clin Biochem. 1982 May;20(5):325-9. doi: 10.1515/cclm.1982.20.5.325.

Abstract

In the context of diagnostic procedures for congenital hyperammonaemias a methods is described for the determination of N-acetylglutamate synthetase in human liver tissue homogenates. The method uses [14C-U] glutamate and acetyl CoA as substrates. The reaction product, N-acetylglutamate is separated from the substrate L-glutamate by chromatography on Extrelut. In a subsequent step on ITLC-SG ready plates N-acetylglutamate is separated from other labeled metabolites such as Krebs cycle intermediates. The recovery of N-acetylglutamate was 97.8%. The precision within run and between days was 8.5% (CV) and 9.6% (CV) respectively. Reference values were established for adult human liver.

摘要

在先天性高氨血症的诊断程序背景下,描述了一种用于测定人肝组织匀浆中N - 乙酰谷氨酸合成酶的方法。该方法使用[14C - U]谷氨酸和乙酰辅酶A作为底物。反应产物N - 乙酰谷氨酸通过在硅藻土柱上层析与底物L - 谷氨酸分离。在随后的ITLC - SG预制板步骤中,N - 乙酰谷氨酸与其他标记代谢物如三羧酸循环中间体分离。N - 乙酰谷氨酸的回收率为97.8%。批内和批间精密度分别为8.5%(变异系数)和9.6%(变异系数)。建立了成人肝脏的参考值。

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