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一种消除蛋白质测定洛氏法中干扰因素的方法。

A procedure for eliminating interferences in the lowry method of protein determination.

作者信息

Rodríguez-Vico F, Martínez-Cayuela M, García-Peregrín E, Ramírez H

机构信息

Department of Biochemistry and Molecular Biology, University of Granada, Spain.

出版信息

Anal Biochem. 1989 Dec;183(2):275-8. doi: 10.1016/0003-2697(89)90479-x.

Abstract

A modification of the Lowry assay for the quantitative protein measurement in the presence of interfering materials has been developed. The method is based on a precipitation with a single-phase hexane:isopropanol solvent system and later resuspension of protein pellets with sodium dodecyl sulfate and deoxycholate. The new procedure eliminates the interference caused by Triton X-100, phospholipids, or dithiothreitol providing yields higher than 95% and seems to be especially suitable for protein determination on membrane preparations in samples with small volumes and/or very low protein concentrations.

摘要

已开发出一种改良的洛瑞法,用于在存在干扰物质的情况下进行蛋白质定量测定。该方法基于用单相己烷:异丙醇溶剂系统进行沉淀,随后用十二烷基硫酸钠和脱氧胆酸盐将蛋白质沉淀重悬。新方法消除了由 Triton X-100、磷脂或二硫苏糖醇引起的干扰,产率高于 95%,似乎特别适用于对小体积和/或蛋白质浓度极低的样品中的膜制剂进行蛋白质测定。

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