一种快速分离线粒体DNA的方法

Earl G. Zimmerman, Darrin R. Akins, John V. Planz, Michael J. Schurr
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引用次数: 12

摘要

描述了一种从动物组织中快速分离线粒体DNA (mtDNA)的技术,该技术消除了使用氯化铯梯度超离心分离核和mtDNA的耗时。该方法利用DNA酶消化核DNA,然后裂解线粒体并随后提取蛋白质,得到相对纯净的mtDNA。每克肝组织中mtDNA含量可达5 μg,用限制性内切酶和溴化乙啶染色进行5次消化的适宜产率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rapid procedure for isolating mitochondrial DNA

A technique for the rapid isolation of mitochondrial DNA (mtDNA) from animal tissues is described that eliminates the time-consuming separation of nuclear and mtDNAs using cesium chloride gradient ultracentrifugation. The procedure utilizes digestion of the nuclear DNA with DNase, after which lysis of mitochondria and subsequent extraction of proteins results in relatively pure mtDNA. Up to 5 μg of mtDNA per gram of liver tissue resulted, a suitable yield for five digests with restriction enzymes and staining with ethidium bromide.

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