Results 311 to 320 of about 526,892 (336)

SDS Polyacrylamide Gel Electrophoresis of Proteins

2003
Probably the most widely used of techniques for analyzing mixtures of proteins is SDS polyacrylamide gel electrophoresis. In this technique, proteins are reacted with the anionic detergent, sodium dodecylsulfate (SDS, or sodium lauryl sulfate) to form negatively charged complexes.
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Gradient SDS Polyacrylamide Gel Electrophoresis

2003
The preparation of fixed-concentration polyacrylamide gels has been described in Chapter 6. However, the use of polyacrylamide gels that have a gradient of increasing acrylamide concentration (and hence decreasing pore size) can sometimes have advantages over fixed-concentration acrylamide gels. During electrophoresis in gradient gels, proteins migrate
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Polyacrylamide Temperature Gradient Gel Electrophoresis

2013
Temperature Gradient Gel Electrophoresis (TGGE) is a form of electrophoresis in which temperature gradient is used to denature molecules as they move through either acrylamide or agarose gel. TGGE can be applied to analyze DNA, RNA, protein-DNA complexes, and, less commonly, proteins.
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Preparative electrophoresis on polyacrylamide gel

Analytical Biochemistry, 1964
D, RACUSEN, N, CALVANICO
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SIMPLIFIED “DISC” (POLYACRYLAMIDE GEL) ELECTROPHORESIS*

Annals of the New York Academy of Sciences, 1964
SummaryCross‐linked homogeneous 5 per cent polyacrylamide gel in rod form is a convenient medium for sharp analytical electrophoretic separation in microgram quantities of most serum proteins and of many biological ampholytes.
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Neutral Polyacrylamide Gel Electrophoresis

Cold Spring Harbor Protocols, 2006
Joseph, Sambrook, David W, Russell
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Polyacrylamide Gel Electrophoresis

2022
Kamal Gandhi, Neelima Sharma, Priyae Brath Gautam, Rajan Sharma, Bimlesh Mann, Vanita Pandey   +5 more
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Electrophoresis of DNA in Nondenaturing Polyacrylamide Gels

2003
For the majority of purposes, such as restriction mapping and sizing of cloned fragments, electrophoresis of DNA in horizontal agarose gels is perfectly adequate. As the size of the fragments of interest decreases to below 1000 base pairs (bp), however, the resolution deteriorates significantly, and an alternative is required.
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Polyacrylamide gel electrophoresis of DNA

Analytical Biochemistry, 1972
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SDS polyacrylamide gel electrophoresis

Trends in Biochemical Sciences, 2000
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