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通过十二烷基硫酸钠凝胶电泳分离超出常规大小限制的DNA分子。

Separation of the DNA molecules beyond conventional size limits by gel electrophoresis with sodium dodecyl sulfate.

作者信息

Tas S

机构信息

Department of Pathology, Faculty of Medicine, Kuwait University, Safat.

出版信息

Anal Biochem. 1990 Jul;188(1):33-7. doi: 10.1016/0003-2697(90)90524-d.

Abstract

Electrophoretic mobility of DNA through polyacrylamide as well as agarose gels is greatly increased by sodium dodecyl sulfate (SDS). DNA molecules well beyond the conventionally separable size limits are separated readily and rapidly by gel electrophoresis with SDS in a conventional static electric field. Furthermore in optimal concentration gels DNA molecules of similar molecular sizes are separated better from one another in the presence of SDS than without it. Evidence is presented that SDS may act at least in part by altering conformation of DNA. This simple and readily available means for high resolution separation of hitherto impossible sizes of DNA molecules in polyacrylamide and agarose gels in an ordinary static electric field should find general use in molecular genetic analyses. Structural analyses of DNA-protein complexes are also facilitated by virtue of the simultaneous separation of the DNA and protein components on the same gel lane.

摘要

十二烷基硫酸钠(SDS)可显著提高DNA在聚丙烯酰胺凝胶和琼脂糖凝胶中的电泳迁移率。在传统的静电场中,使用含有SDS的凝胶电泳能够轻松且快速地分离远远超出传统可分离尺寸限制的DNA分子。此外,在最佳浓度的凝胶中,存在SDS时,相似分子大小的DNA分子比不存在SDS时能更好地相互分离。有证据表明,SDS至少部分是通过改变DNA的构象起作用的。这种在普通静电场中,利用简单且易于获得的方法在聚丙烯酰胺凝胶和琼脂糖凝胶中对迄今无法分离的大小的DNA分子进行高分辨率分离,应该会在分子遗传学分析中得到广泛应用。由于能在同一凝胶泳道上同时分离DNA和蛋白质成分,DNA - 蛋白质复合物的结构分析也因此变得更加容易。

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