Effect of strand bias, sequence specificity and cisplatin–DNA adduct position on Ku binding

Copyright information:Taken from "Differential activation of DNA-PK based on DNA strand orientation and sequence bias"Nucleic Acids Research 2005;33(1):152-161.Published online 07 Jan 2005PMCID:PMC546145.© 2005, the authors © () Competition binding assays were performed in 20 μl reactions...

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Hauptverfasser: Pawelczak, Katherine S., Andrews, Brooke J., Turchi, John J.
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Sprache:eng
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Zusammenfassung:Copyright information:Taken from "Differential activation of DNA-PK based on DNA strand orientation and sequence bias"Nucleic Acids Research 2005;33(1):152-161.Published online 07 Jan 2005PMCID:PMC546145.© 2005, the authors © () Competition binding assays were performed in 20 μl reactions and contained 2.5 nM P-labeled double-stranded 2.1/2.2 DNA and 5 nM Ku. Increasing concentrations of the SA-bound competitor DNA (3P/3B), 5, 50 and 200 nM is indicated by the triangles. Controls for the assay include P-labeled double-stranded 2.1/2.2 DNA alone (lane 1) and P-labeled double-stranded 2.1/2.2 DNA with 5 nM Ku in the absence of any competitor (lane 2). () Competition assays were carried out identically to those in (A) except reactions included 5P/5B competitor DNA.
DOI:10.6084/m9.figshare.50053