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Electrophoretic Mobility Shift Assay Using Radiolabeled DNA Probes.

DNA-PROTEIN INTERACTIONS: PRINCIPLES AND PROTOCOLS, 4TH EDITION(2015)

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Abstract
Electrophoretic mobility shift assays (EMSA) have proven their usefulness for studying interactions between biological molecules. In the present protocol, a purified protein of interest is mixed with a 5'-end radiolabeled DNA probe. The bound complexes are separated by electrophoretic migration through a polyacrylamide gel and detected with a phosphorimager. The applications of EMSA are diverse, from thermodynamic and kinetic analyses to observation of bending and other conformational changes, stoichiometric inferences, or insights into cooperative protein binding.
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Key words
DNA probe labeling,EMSA,Electrophoretic mobility shift assay,Gel retardation,Gel shift,Native polyacrylamide gel,Phosphorus-32,Protein–DNA interactions
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