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变性聚丙烯酰胺凝胶电泳

Denaturing polyacrylamide gel electrophoresis.

作者信息

Albright L M, Slatko B E

机构信息

New England Biolabs, Beverly, Massachusetts, USA.

出版信息

Curr Protoc Nucleic Acid Chem. 2001 May;Appendix 3:Appendix 3B. doi: 10.1002/0471142700.nca03bs00.

DOI:10.1002/0471142700.nca03bs00
PMID:18428811
Abstract

Thin polyacrylamide gels that contain a high concentration of urea as a denaturant are capable of resolving short (<500 nucleotides) single-stranded fragments of DNA or RNA that differ in length by as little as one nucleotide. Such gels are uniquely suited for nucleic acid sequence analysis, which is required, for instance, for all footprinting protocols. Thicker gels are often used to purify oligonucleotides. This appendix describes the pouring, running, and processing of a typical sequencing gel, which is 40 cm long with a uniform thickness of 0.4 mm, containing 7 M urea and 4% to 8% acrylamide.

摘要

含有高浓度尿素作为变性剂的薄聚丙烯酰胺凝胶,能够分离长度相差仅一个核苷酸的短(<500个核苷酸)DNA或RNA单链片段。这种凝胶特别适合核酸序列分析,例如所有足迹分析方案都需要这种分析。较厚的凝胶通常用于纯化寡核苷酸。本附录描述了一种典型测序凝胶的灌制、运行和处理方法,该凝胶长40厘米,厚度均匀为0.4毫米,含有7M尿素和4%至8%的丙烯酰胺。

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1
Denaturing polyacrylamide gel electrophoresis.变性聚丙烯酰胺凝胶电泳
Curr Protoc Nucleic Acid Chem. 2001 May;Appendix 3:Appendix 3B. doi: 10.1002/0471142700.nca03bs00.
2
Denaturing polyacrylamide gel electrophoresis.变性聚丙烯酰胺凝胶电泳
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Denaturing gel electrophoresis for sequencing.用于测序的变性凝胶电泳
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Denaturing urea polyacrylamide gel electrophoresis (Urea PAGE).变性尿素聚丙烯酰胺凝胶电泳(尿素聚丙烯酰胺凝胶电泳)。
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Identification and suppression of secondary structures formed from deoxy-oligonucleotides during electrophoresis in denaturing polyacrylamide-gels.变性聚丙烯酰胺凝胶电泳过程中脱氧寡核苷酸形成的二级结构的鉴定与抑制
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Purification of DNA Oligos by denaturing polyacrylamide gel electrophoresis (PAGE).通过变性聚丙烯酰胺凝胶电泳(PAGE)纯化DNA寡核苷酸。
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High-resolution polyacrylamide gel electrophoresis of oligonucleotides using L-histidine buffer.使用L-组氨酸缓冲液对寡核苷酸进行高分辨率聚丙烯酰胺凝胶电泳。
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Optimization of polyacrylamide gel electrophoresis conditions used for sequencing mixed oligodeoxyribonucleotides.用于测序混合寡聚脱氧核糖核苷酸的聚丙烯酰胺凝胶电泳条件的优化。
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