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从酸脲- Triton和十二烷基硫酸钠聚丙烯酰胺凝胶中快速有效地进行组蛋白的蛋白质免疫印迹分析:两种不同方法,取决于后续的定性或定量分析。

Rapid and effective western blotting of histones from acid-urea-Triton and sodium dodecyl sulfate polyacrylamide gels: two different approaches depending on the subsequent qualitative or quantitative analysis.

作者信息

Thiriet C, Albert P

机构信息

Laboratoire de Biologie Cellulaire, Université de Reims, France.

出版信息

Electrophoresis. 1995 Mar;16(3):357-61. doi: 10.1002/elps.1150160161.

Abstract

An improved method for the electrophoretic transfer of histones from sodium dodecyl sulfate (SDS) and acetic acid-urea-Triton X-100 (AUT) polyacrylamide gels onto nitrocellulose membranes is described. In the case of SDS-gels, it was not essential to equilibrate them before transfer while for the AUT-gels, an equilibration step is essential to prevent the interference of Triton X-100 with the binding of histones to nitrocellulose. Transfer efficiency was different for different histone classes. Two procedures were developed: (1) one suitable for qualitative studies, and (ii) another for quantitative transfer.

摘要

本文描述了一种改进的方法,用于将组蛋白从十二烷基硫酸钠(SDS)和醋酸 - 尿素 - 曲拉通X - 100(AUT)聚丙烯酰胺凝胶电泳转移至硝酸纤维素膜上。对于SDS凝胶,转移前无需平衡;而对于AUT凝胶,平衡步骤必不可少,以防止曲拉通X - 100干扰组蛋白与硝酸纤维素的结合。不同组蛋白类别的转移效率有所不同。开发了两种方法:(1)一种适用于定性研究,(2)另一种适用于定量转移。

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