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Updated: Jun 23, 2026

An Optimized Protocol for Electrophoretic Mobility Shift Assay Using Infrared Fluorescent Dye-labeled Oligonucleotides
Published on: November 29, 2016
The cruciform DNA mobility shift assay: a tool to study proteins that recognize bent DNA
Victor Y Stefanovsky1, Tom Moss
1Department of Medical Biology, Cancer Research Centre, Hôtel-Dieu de Québec, 9 rue McMahon Québec, QC, Canada G1R 2J6.
Abstract:
So-called architectural DNA binding proteins such as those of the HMGB-box family induce DNA bending and kinking. However, these proteins often display only a weak sequence preference, making the analysis of their DNA binding characteristics difficult if not impossible in a standard electrophoretic mobility assay (EMSA). In contrast, such proteins often bind prebent DNAs with high affinity and specificity. A synthetic cruciform DNA structure will often provide an ideal binding site for such proteins, allowing their affinities for both bent and linear DNAs to be directly and simply determined by a modified form of EMSA.
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