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An electrophoretic color marker is used to monitor the progress of agarose gel electrophoresis and polyacrylamide gel electrophoresis (PAGE) since DNA, RNA, and most proteins are colourless. They are also referred to as tracking dyes, and are frequently present in loading dyes as well as molecular weight ladders.
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Sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-
PAGE) is a very common and elegant molecular biology technique
for analyzing and separating complex mixture of proteins and other
biological macromolecules by using a discontinuous polyacryl-
amide gel as a support medium and sodium dodecyl sulfate (SDS)
to denature proteins [1, 2]. To detect a protein band on the elec-
trophoretic gel, either a poststaining or prestaining technique is
applied. In conventional poststaining technique, after electropho-
retic separation, the gel is usually stained by immersing it in a dye
such as Amido Black, Coomassie Brilliant Blue, or silver stain.
Silver stains are more sensitive as compared to the other two, how-
ever, these techniques have its own limitations: (1) long destaining
time is required for obtaining clear background; (2) faint bands are
difficult to analyze due to background from some of the retained
dyes, thus affecting the quality of resolution [3]. Alternatively, pro-
teins can be fluorescently labeled with dansyl chloride,
2-methoxy-2,4,-diphenyl-3(2H) furanone, or fluorescamine and
can be visualized by ultraviolet illumination [4–6]. These simple
staining techniques help to avoid the problem of altered electro-
phoretic mobility on the gels[1]
Color Markers for Electrophoresis. (1997). Science, 277(5328), 979–979. http://www.jstor.org/stable/2892922
Chang, Hsu, H.-Y., & Lee, H.-J. (2005). Dye-free protein molecular weight markers. Electrophoresis, 26(16), 3062–3068. https://doi.org/10.1002/elps.200500041
Compton, Lapp, S. A., & Pedemonte, R. (2002). Generation of multicolored, prestained molecular weight markers for gel electrophoresis. Electrophoresis, 23(19), 3262–3265. https://doi.org/10.1002/1522-2683(200210)23:193.0.CO;2-8
José Bubis, Proposal of a laboratory course dedicated to the generation of protein molecular weight standards for sodium dodecyl sulfate‐polyacrylamide gel electrophoresis, Biochemistry and Molecular Biology Education, 10.1002/bmb.21476, 49, 3, (353-360), (2020)
.In order to visualize nucleic acid molecules in agarose gels, ethidium bromide or SYBR Green are commonly used dyes. Illumination of the agarose gels with 300-nm UV light is subsequently used for visualizing the stained nucleic acids. Throughout this chapter, the common methods for staining and visualization of DNA are described in details.
- ^ Kumar, Gaurav (2018). "Multicolored Prestained Standard Protein Marker Generation Using a Variety of Remazol Dyes for Easy Visualization of Protein Bands During SDS-PAGE". Methods in Molecular Biology (Clifton, N.J.). 1853: 19–25. doi:10.1007/978-1-4939-8745-0_3. ISSN 1940-6029. PMID 30097925.
- ^ Ylmaz, Muhittin; Ozic, Cem; Gok, lhami (2012-04-04), Magdeldin, Sameh (ed.), "Principles of Nucleic Acid Separation by Agarose Gel Electrophoresis", Gel Electrophoresis - Principles and Basics, InTech, doi:10.5772/38654., ISBN 978-953-51-0458-2, retrieved 2023-05-11
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