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Lithium dodecyl sulfate, sodium dodecyl sulfate-agarose gel electrophoresis for separating proteins according to molecular weight

机译:十二烷基硫酸钠,十二烷基硫酸钠-琼脂糖凝胶电泳根据分子量分离蛋白质

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摘要

We have improved the agarose gel electrophoresis method reported previously for size-dependent separation of proteins. Good resolution in protein separation was achieved using a novel agarose gel, containing both sodium dodecyl sulfate (SDS) and lithium dodecyl sulfate (LDS). The gel was divided into stacking and separating gels. We determined the optimal conditions for horizontal gel electrophoresis to be a voltage of 100 V for the separating gel and 50 V for the stacking gel, in an electrophoretic buffer solution of 25 mM Tris-190 mM glycine containing 0.03% LDS and 0.02% SDS (pH 8.3), which was also used to make the agarose gel. Separation of proteins in the molecular weight range 14.2-205 K and of the proteins in human serum showed good resolution under these conditions. This method should be useful for clinical laboratories because it is simple and requires little bench space.
机译:我们已经改进了先前报道的琼脂糖凝胶电泳方法,用于蛋白质的大小依赖性分离。使用新型的琼脂糖凝胶,同时包含十二烷基硫酸钠(SDS)和十二烷基硫酸锂(LDS),可以实现蛋白质分离的良好分离度。将该凝胶分为堆积凝胶和分离凝胶。在25 mM Tris-190 mM甘氨酸含有0.03%LDS和0.02%SDS的电泳缓冲溶液中,我们确定水平凝胶电泳的最佳条件是分离凝胶的电压为100 V,堆叠凝胶的电压为50 V( pH 8.3),也用于制备琼脂糖凝胶。在这些条件下,分子量范围为14.2-205 K的蛋白质和人血清中蛋白质的分离显示出良好的分离度。该方法简单易行,所需的工作台空间很小,因此对临床实验室应有用。

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