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• W2141036280 abstract "We have developed a sensitive, non-radioactive method to assess the interaction of transcription factors/DNA-binding proteins with DNA. We have modified the traditional radiolabeled DNA gel mobility shift assay to incorporate a DNA probe end-labeled with a Texas-red fluorophore and a DNA-binding protein tagged with the green fluorescent protein to monitor precisely DNA-protein complexation by native gel electrophoresis. We have applied this method to the DNA-binding proteins telomere release factor-1 and the sex-determining region-Y, demonstrating that the method is sensitive (able to detect 100 fmol of fluorescently labeled DNA), permits direct visualization of both the DNA probe and the DNA-binding protein, and enables quantitative analysis of DNA and protein complexation, and thereby an estimation of the stoichiometry of protein-DNA binding." @default.
• W2141036280 created "2016-06-24" @default.
• W2141036280 creator A5029725982 @default.
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• W2141036280 date "2006-08-01" @default.
• W2141036280 modified "2023-09-23" @default.
• W2141036280 title "Quantitative analysis of DNA-protein interactions using double-labeled native gel electrophoresis and fluorescence-based imaging" @default.
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• W2141036280 doi "https://doi.org/10.1002/elps.200500872" @default.
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