在琼脂糖凝胶电泳中正确使用 DNA 染料。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Ling-Jin Tuo, Teng Zhang, Guo-Qing Chen, Yuan Liu, Cheng Zhao, Shi-Wen Jiang
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引用次数: 0

摘要

在琼脂糖凝胶电泳(AGE)中,有多种染料可通过预染色或后染色的方法显现 DNA 条带。DNA 染料用户指南通常指出,染料与 DNA 的结合会影响 DNA 在电泳中的迁移率,因此建议采用后染色法来准确测量 DNA 的大小。然而,出于方便、实时观察 DNA 条带和/或使用极少量染料等原因,许多 AGE 执行者更喜欢预染色程序。染料对 DNA 迁移性的不利影响以及与之相关的 DNA 大小测量不准确的风险往往被 AGE 执行者所忽视。在此,我们定量测定了常用染料(包括 GelRed、溴化乙锭(EB)和 Gold View)对 DNA 迁移的影响。结果表明,GelRed 和 EB 的预染色会明显减慢 DNA 的迁移速度,导致对样本 DNA 大小的高估高达 39.1%,而 Gold View 的影响则很小。DNA 迁移速度随着染料浓度的增加而减慢,直到染料浓度达到饱和水平时才趋于平稳。因此,为了利用预染色的优势,DNA 样品和 DNA 标记都应始终使用饱和水平的 DNA 染料,以确保 DNA 大小的公平比较。此外,在染色后检测 DNA 条带方面,GelRed 和 EB 的灵敏度远高于 Gold View。现将这些常用染料的饱和浓度、成本考虑因素和其他有用特性进行总结,供 AGE 执行人员参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proper application of DNA dyes in agarose gel electrophoresis

Various dyes are used to visualize DNA bands in agarose gel electrophoresis (AGE) by the methods of pre- or post-staining. The DNA dye user's guides generally state that the binding of the dye to DNA will affect DNA mobility in electrophoresis, thus recommending post-staining for accurate measurement of DNA size. However, many AGE performers prefer pre-staining procedures for reasons such as convenience, real-time observation of DNA bands, and/or the use of a minimal amount of dye. The detrimental effect of the dye on DNA mobility and the associated risk for inaccurate measurement of DNA size are often overlooked by AGE performers. Here we quantitatively determine the impact on DNA migration imposed by frequently used dyes, including GelRed, ethidium bromide (EB), and Gold View. It was observed that pre-staining with GelRed and EB significantly slowed down DNA migration to cause as much as 39.1% overestimation on the size of sample DNA, whereas Gold View had little effect. The slowdown of DNA migration increased with dye concentration until it plateaued when the dye concentration reached a saturated level. Thus, to take advantage of pre-staining, saturated levels of DNA dyes should always be applied for both DNA samples and DNA markers to ensure a fair comparison of DNA sizes. In addition, GelRed and EB display much higher sensitivity than Gold View in the detection of DNA bands in post-staining. The saturated concentrations, cost considerations, and other useful features of these frequently used dyes are summarized for the information of AGE performers.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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