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蛋白质组分析的经典 2D-PAGE 技术。

Proteome Analysis with Classical 2D-PAGE.

机构信息

Medizinisches Proteom-Center (MPC), Medical Faculty, Ruhr-University Bochum, Bochum, Germany.

Medical Proteome Analysis, Center for Proteindiagnostics (PRODI) Ruhr-University Bochum, Bochum, Germany.

出版信息

Methods Mol Biol. 2021;2228:53-62. doi: 10.1007/978-1-0716-1024-4_5.

Abstract

Two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) is based on the combination of two orthogonal separation techniques. In the first dimension, proteins are separated by their isoelectric point, a technique known as isoelectric focusing (IEF). There are two important variants of IEF, which are carrier-ampholine (CA)-based IEF and immobilized pH-gradient (IPG)-based IEF. In the second dimension, proteins are further separated by their electrophoretic mobility using SDS-PAGE. Finally, proteins can be visualized and quantified by different staining procedures such as Coomassie, silver staining, or fluorescence labeling. This article gives detailed protocols for 2D-PAGE, using both CA- and IPG-based separation in the first dimension.

摘要

二维聚丙烯酰胺凝胶电泳(2D-PAGE)基于两种正交分离技术的结合。在第一维中,蛋白质根据等电点进行分离,这一技术被称为等电聚焦(IEF)。IEF 有两个重要的变体,分别是基于载体两性电解质(CA)的 IEF 和基于固定 pH 梯度(IPG)的 IEF。在第二维中,蛋白质通过 SDS-PAGE 进一步根据其电泳迁移率进行分离。最后,蛋白质可以通过不同的染色程序进行可视化和定量,例如考马斯亮蓝染色、银染或荧光标记。本文详细介绍了使用 CA 和 IPG 分别在第一维和第二维进行分离的 2D-PAGE 的实验方案。

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本文引用的文献

1
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