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用于DNA复制分析的二维琼脂糖凝胶电泳

Two-dimensional agarose gel electrophoresis for analysis of DNA replication.

作者信息

Villwock Sandra K, Aparicio Oscar M

机构信息

Molecular and Computational Biology Program, University of Southern California, 1050 Childs Way, Los Angeles, CA, 90089, USA.

出版信息

Methods Mol Biol. 2014;1205:329-40. doi: 10.1007/978-1-4939-1363-3_19.

Abstract

The initiation, elongation, and termination of DNA replication are each associated with distinct, nonlinear DNA structures that can be resolved and identified by two-dimensional (2D) agarose gel electrophoresis. This method involves: isolation of genomic DNA while preserving fragile replication structures, digestion of the DNA with a restriction enzyme, separation of DNA by size and shape through two distinct stages of agarose gel electrophoresis, and Southern blotting to probe for the specific sequence(s) of interest. The method has been most commonly used to determine the activity level of putative replication origin-containing sequences, and has also been used to analyze replication timing, fork progression, fork pausing, fork stalling and collapse, termination, and recombinational repair.

摘要

DNA复制的起始、延伸和终止均与独特的非线性DNA结构相关,这些结构可通过二维(2D)琼脂糖凝胶电泳进行解析和鉴定。该方法包括:在保留脆弱的复制结构的同时分离基因组DNA,用限制性内切酶消化DNA,通过琼脂糖凝胶电泳的两个不同阶段按大小和形状分离DNA,以及进行Southern印迹以探测感兴趣的特定序列。该方法最常用于确定含假定复制起点序列的活性水平,也已用于分析复制时间、叉形进展、叉形暂停、叉形停滞和崩溃、终止以及重组修复。

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