DNA-PKcs Antibody

Knockdown Validated: DNA-PKcs Antibody [NB100-658]

Knockdown Validated: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection. End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or DNA-PKcs antibody. Data are mean +/- SEM. Image collected and cropped by CiteAb from the following publication (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316416/) licensed under a CC-BY license.

Western Blot: DNA-PKcs Antibody [NB100-658] -

Western Blot: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection(A) Schematic of the NHEJ reporter assay. The repair of two I-SceI-induced DSBs can result in loss of the intervening fragment, which is detected by a CD4+ signal (Rass et al., 2009). CD4+ clones were amplified by PCR (green arrows) across the repair site & sequenced. Repair of the two DSBs can also occur without loss of the intervening fragment, which escapes detection.(B) gammaH2AX foci in GC92 WT & Artemis KO cells treated with siDNA-PKcs or siCtIP. Cells were transfected with I-SceI, & foci were scored in I-SceI+ & I-SceI− cells (identified by immunofluorescence [IF] against I-SceI). Data are mean ± SEM.(C) End joining events in GC92 WT & Artemis KO cells containing the NHEJ reporter substrate. Cells were transfected with RFP or cMyc-Artemis constructs. Events were quantified by the fraction of CD4+ & RFP/cMyc+cells relative to all RFP/cMyc+cells, & results were normalized to WT cells. Data are mean ± SEM.(D) End joining events in GC92 WT & Artemis KO cells treated with siCtIP. Data are mean ± SEM.(E) Distribution of deletion sizes obtained from the sequence analysis of GC92 WT & siLig1/3-treated cells. nt, nucleotide.(F) End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or siDNA-PKcs. Data are mean ± SEM.See also Table S1. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/28132842), licensed under a CC-BY license. Not internally tested by Novus Biologicals.