Sandra Harper, David W. Speicher
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引用次数: 5
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Abstract
This manuscript describes protocols for separation of complex protein samples using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE). Electrophoresis in a single dimension, e.g., 1D SDS polyacrylamide gels, has the potential to rapidly separate hundreds of proteins. When two orthogonal high-resolution electrophoretic methods are efficiently combined in perpendicular dimensions, complex protein mixtures can be separated into thousands of discrete spots. The most common 2D gel separation for intact proteins involves a first-dimensional separation using isoelectric focusing (IEF) followed by separation based on protein size (SDS-PAGE). Currently, most 2D gel studies rely on the use of commercially available immobilized pH gradient (IPG) gels, which provide improved ease of use and reproducibility compared with older methods. IPG gels are available in a range of sizes and different pH ranges. Resolution typically increases as the 2D gel size increases; however, difficulty of use increases sharply and throughput decreases as gel size increases. © 2019 by John Wiley & Sons, Inc.
使用二维聚丙烯酰胺凝胶比较复杂蛋白质样品
本文描述了使用二维聚丙烯酰胺凝胶电泳(2D-PAGE)分离复杂蛋白质样品的方案。单维度电泳,例如,一维SDS聚丙烯酰胺凝胶,具有快速分离数百种蛋白质的潜力。当两种正交的高分辨率电泳方法在垂直维度上有效结合时,复杂的蛋白质混合物可以被分离成数千个离散的点。完整蛋白质最常见的二维凝胶分离包括使用等电聚焦(IEF)进行一维分离,然后根据蛋白质大小进行分离(SDS-PAGE)。目前,大多数2D凝胶研究依赖于使用市售的固定化pH梯度(IPG)凝胶,与旧方法相比,IPG凝胶提供了更好的易用性和可重复性。IPG凝胶有多种尺寸和不同的pH值范围。分辨率通常随着2D凝胶尺寸的增加而增加;然而,随着凝胶尺寸的增加,使用难度急剧增加,吞吐量下降。©2019 by John Wiley &儿子,Inc。
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