首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >HIGH RESOLUTION, STANDARD FORMAT TWO-DIMENSIONAL PROTEIN ELECTROPHORESIS USING DISPOSABLE GLASS MICROPIPETTES AND NON-DEDICATED EQUIPMENT
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HIGH RESOLUTION, STANDARD FORMAT TWO-DIMENSIONAL PROTEIN ELECTROPHORESIS USING DISPOSABLE GLASS MICROPIPETTES AND NON-DEDICATED EQUIPMENT

机译:使用一次性玻璃微管和非专用设备进行高分辨率,标准格式的二维蛋白质电泳

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摘要

A method for high resolution, two-dimensional polyacrylamide gel electrophoresis (PAGE) of proteins on a standard format that utilizes nondedicated electrophoretic equipment is described. This method combines key features of various previous protocols into an improved approach which can readily be applied by persons experienced only in sodium dodecyl sulfate (SDS)-PAGE. The method yields high-quality two-dimensional protein separations that are reliably reproducible and uniform between different analyses. High protein resolution is attained and preserved primarily by facilitating the execution of the first isoelectric focusing (IEF) dimension and streamlining the initiation of the second (SDS-PAGE) dimension. Important features of this method include the use of piperazine diacrylate cross-linker, disposable glass micropipettes, and conical sample chambers in the IEF dimension. In addition, the equilibration of the first-dimensional gels is accomplished at the same time the gels are loaded onto the second dimension. Loss of protein resolution due to diffusion after the end of the first dimension is reduced by minimizing the time required to load the SDS-PAGE dimension. The method is versatile and adaptable to the analysis of one or many samples. The high degree of resolution, reproducibility and uniformity attained by this method are sufficient to abrogate the need for dedicated equipment in most applications. [References: 18]
机译:描述了一种利用非专用电泳设备以标准格式对蛋白质进行的高分辨率二维聚丙烯酰胺凝胶电泳(PAGE)的方法。该方法将先前各种协议的关键特征组合到一种改进的方法中,该方法可以被仅在十二烷基硫酸钠(SDS)-PAGE中有经验的人员轻松应用。该方法可产生高质量的二维蛋白质分离,该分离可可靠地重现,并且在不同分析之间保持一致。通过促进执行第一个等电聚焦(IEF)尺寸和简化第二个(SDS-PAGE)尺寸的起始尺寸,可以实现并保持较高的蛋白质分辨率。该方法的重要特征包括使用IEF尺寸的哌嗪二丙烯酸酯交联剂,一次性玻璃微量移液器和锥形样品室。另外,第一维凝胶的平衡是在将凝胶加载到第二维上的同时完成的。通过最小化加载SDS-PAGE尺寸所需的时间,减少了因第一维尺寸结束后的扩散而导致的蛋白质分辨率损失。该方法用途广泛,适用于分析一个或多个样品。通过这种方法获得的高分辨率,重现性和均匀性足以消除大多数应用中对专用设备的需求。 [参考:18]

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