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DNA的定量凝胶电泳:限制内切酶消化重叠条带的分辨率

Quantitative gel electrophoresis of DNA: resolution of overlapping bands of restriction endonuclease digests.

作者信息

Ribeiro E A, Sutherland J C

机构信息

Biology Department, Brookhaven National Laboratory, Upton, New York 11973.

出版信息

Anal Biochem. 1991 Apr;194(1):174-84. doi: 10.1016/0003-2697(91)90165-p.

Abstract

Accurate quantitation of the distribution of DNA digested to completion by a restriction endonuclease and separated in an electrophoretic gel is greatly facilitated by electronic imaging systems employing charge-coupled device detectors. Such quantitation permits the extraction of more accurate values of the lengths of both the parent molecular species and the fragments produced by a restriction endonuclease. We describe a method that determines the number of components in bands containing two or more daughter fragments that are of similar length and hence not resolved by gel electrophoresis. We also report a constrained deconvolution procedure based on the equal number of daughter molecules in a terminal digestion by a restriction endonuclease that resolves the distribution of each of the overlapping species in a composite band on a gel and hence increases the accuracy of the lengths assigned to each.

摘要

采用电荷耦合器件探测器的电子成像系统极大地促进了对经限制性内切酶完全消化并在电泳凝胶中分离的DNA分布的准确定量。这种定量能够提取出更准确的亲本分子物种以及由限制性内切酶产生的片段的长度值。我们描述了一种方法,该方法可确定包含两个或更多长度相似因而无法通过凝胶电泳分离的子片段的条带中的组分数量。我们还报告了一种基于限制性内切酶末端消化中相等数量子分子的约束反卷积程序,该程序可解析凝胶上复合条带中每个重叠物种的分布,从而提高分配给每个物种的长度的准确性。

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