Rapid DNA purification for restriction fragment length polymorphism analysis

Bertil Lindblom , Gunilla Holmlund
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引用次数: 60

Abstract

This paper describes a method for isolation of DNA from blood samples involving a rapid chemical disintegration of proteins with 8 M urea and with a minimum of exposure to phenol. The DNA is further desalted and purified on Sephadex G-25 prepacked disposable columns. DNA isolated in this way was pure enough to be immediately cleaved by restriction enzymes.

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快速DNA纯化用于限制性片段长度多态性分析
本文描述了一种从血液样本中分离DNA的方法,该方法涉及用8 M尿素快速化学分解蛋白质,并以最小的苯酚暴露。DNA在Sephadex G-25预包装一次性色谱柱上进一步脱盐和纯化。用这种方法分离的DNA足够纯净,可以立即被限制性内切酶切割。
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Gene targeting in murine embryonic stem cells: Introduction of specific alterations into the mammalian genome A solution hybridization method for quantification of mRNAs: Determining the amount and stability of oncogene mRNA The use of transgenic mice for short-term, in vivo mutagenicity testing Author index volume 7 Subject index volume 7
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