改进的sds -聚丙烯酰胺凝胶电泳可分离3.5-200kDa范围内的多肽。

Z Khalkhali-Ellis
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引用次数: 22

摘要

广泛的多肽,3.5-200kDa,在一个低丙烯酰胺和交联凝胶7.7% T, 2.6% C的分辨率描述在这里。Laemmli(4)最初的不连续SDS聚丙烯酰胺凝胶电泳(SDS- page)系统经过改进,增加了堆叠和分解凝胶的离子强度,并用Schagger和von Jagow(7)所描述的三酸阴极缓冲液取代了通常的甘氨酸缓冲液。该系统具有在单一低丙烯酰胺浓度和交联凝胶上具有足够波段分辨率的大范围蛋白质分离的优势。此外,增加的凝胶离子浓度允许更高的蛋白质和盐负荷,并使该系统适合于制备工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An improved SDS-polyacrylamide gel electrophoresis for resolution of peptides in the range of 3.5-200kDa.

Resolution of a wide range of polypeptides, 3.5-200kDa, on a single low acrylamide and cross linkage gel of 7.7% T, 2.6% C is described here. Laemmli's (4) original discontinuous SDS polyacrylamide gel electrophoresis (SDS-PAGE) system is modified by increasing the ionic strength of both stacking and resolving gels, and replacing the usual glycine buffer with a tricine cathode buffer as described by Schagger and von Jagow (7). This system offers the advantage of a wide range of protein fractionation, with sufficient band resolution, on a single, low acrylamide concentration and cross linkage gel. Moreover, increased gel ionic concentration allows higher protein and salt load, and renders this system suitable for preparative work.

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