聚丙烯酰胺凝胶电泳(SDS-PAGE)

Sean R. Gallagher
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引用次数: 0

摘要

电泳用于分离复杂的蛋白质混合物(例如,来自细胞、亚细胞组分、柱组分或免疫沉淀物),研究亚基组成,验证蛋白质样品的均匀性,并纯化用于进一步应用的蛋白质。在聚丙烯酰胺凝胶电泳中,蛋白质响应电场通过聚丙烯酰胺凝胶基质中的孔隙迁移;孔径随丙烯酰胺浓度的增加而减小。孔隙大小与蛋白质的电荷、大小和形状的结合决定了蛋白质的迁移速率。在本单元中,描述了在变性条件下(即在十二烷基硫酸钠(SDS)存在下)进行不连续凝胶电泳的标准Laemmli方法。支持方案包括凝胶的铸造,使用蛋白质的电泳迁移率计算分子质量,以及通过重结晶纯化SDS。咕咕叫。Protoc。基本的实验室。科技,6:7.3.1-7.3.28。©2012 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SDS-Polyacrylamide Gel Electrophoresis (SDS-PAGE)

Electrophoresis is used to separate complex mixtures of proteins (e.g., from cells, subcellular fractions, column fractions, or immunoprecipitates), investigate subunit compositions, verify homogeneity of protein samples, and purify proteins for use in further applications. In polyacrylamide gel electrophoresis, proteins migrate in response to an electrical field through pores in a polyacrylamide gel matrix; pore size decreases with increasing acrylamide concentration. The combination of pore size and protein charge, size, and shape determines the migration rate of the protein. In this unit, the standard Laemmli method is described for discontinuous gel electrophoresis under denaturing conditions, i.e., in the presence of sodium dodecyl sulfate (SDS). Support protocols cover the casting of gels, calculation of molecular mass using the electrophoretic mobility of a protein, and purification of SDS by recrystallization. Curr. Protoc. Essential Lab. Tech. 6:7.3.1-7.3.28. © 2012 by John Wiley & Sons, Inc.

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