Purification of bacteriophage DNA by gel filtration chromatography

Ana González, Jaime Gómez-Márquez
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引用次数: 5

Abstract

Two fast and effective methods for high-scale purification of linear phage λ DNA and circular double-stranded M13 replicative form are presented. A substantial reduction of time is attained by avoiding the long-term CsCl gradient centrifugations and dialysis common to standard procedures. Biologically active DNA preparations, free of chromosomal DNA and RNA, are obtained by including a simple gel filtration chromatography as the last step of purification. Yields are comparable to those from previously described methods.

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凝胶过滤色谱法纯化噬菌体DNA
提出了两种快速有效的大规模纯化线性噬菌体λ DNA和环状双链M13复制形式的方法。通过避免标准程序中常见的长期CsCl梯度离心和透析,大大减少了时间。生物活性的DNA制剂,不含染色体DNA和RNA,通过包括一个简单的凝胶过滤层析作为纯化的最后一步获得。产量与以前描述的方法相当。
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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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