琼脂糖凝胶电泳

Jennifer A. Armstrong, Joseph R. Schulz
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引用次数: 16

摘要

琼脂糖凝胶电泳,分离和大小线性DNA和RNA片段,可以说是分子生物学中最基本和最重要的技术。它通常用于PCR产物、质粒DNA和限制性内切酶酶切产物的分析。这是通过northern和Southern blots分析特定DNA和RNA片段的第一步。在本单元中,我们提供书面说明和摄影图像,以使读者从准备第一个琼脂糖凝胶到分析结果和确定样品DNA的大小。我们包括两种方案:琼脂糖凝胶电泳(通常用于分析DNA)和变性凝胶电泳(用于分析RNA)。我们将每个方案分为四个基本步骤:(1)制备和浇注琼脂糖凝胶;(2)样品的制备和上样;(3)运行琼脂糖凝胶;(4)使用溴化乙啶荧光染色剂对凝胶进行染色,使DNA和RNA可视化。©2015 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Agarose Gel Electrophoresis

Agarose gel electrophoresis, which separates and sizes linear DNA and RNA fragments, is arguably the most basic and essential technique in molecular biology. It is commonly employed for analysis of PCR products, plasmid DNA, and products of restriction enzyme digestion. It is the first step for analysis of specific DNA and RNA fragments by northern and Southern blots. In this unit, we provide both written instructions and photographic images to take the reader from preparing a first agarose gel to analyzing results and determining the size of sample DNA. We include two protocols: agarose gel electrophoresis (commonly used to analyze DNA) and denaturing gel electrophoresis (for analyzing RNA). We have divided each protocol into four basic steps: (1) preparing and pouring the agarose gel; (2) preparing and loading samples; (3) running the agarose gel; and (4) staining the gel using the fluorescent stain ethidium bromide to visualize DNA and RNA. © 2015 by John Wiley & Sons, Inc.

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