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Image Search Results
Journal: bioRxiv
Article Title: WRN Helicase is a Synthetic Lethal Target in Microsatellite Unstable Cancers
doi: 10.1101/502070
Figure Lengend Snippet: a , IB of γH2AX, phospho(T86)- and total-Chk2, WRN, and GAPDH in representative cell lines after CRISPR/Cas9-mediated WRN depletion. b , γH2AX IF of representative cell lines after delivery of indicated sgRNAs. Scale bar = 50 μm. c , Quantification of nuclear γH2AX staining intensity per cell. d , phospho-ATM (S1981) IF of representative cell lines after delivery of indicated sgRNAs. Scale bar = 50 μm. e , IB of γH2AX, phospho(T86)- and total-Chk2, and GAPDH after RNAi-mediated WRN knockdown. f , IB of γH2AX, WRN, MLH1, MSH3, GAPDH in HCT116 with or without MMR restoration after lentiviral transduction of indicated shRNAs. g , Relative viability of HCT116 cells with and without MMR restoration 7 days after lentiviral delivery of the indicated shRNAs. Values are presented as means ± SE (n = 6). (*) p < 0.01; (**) p < 0.001; (***) p < 0.0002 by two-tailed Student’s t -test. h , WRN IF of representative cell lines. Scale bar = 20 μm i , Quantitative analysis of WRN colocalization to the nucleolar marker, fibrillarin, by Pearson’s colocalization coefficients. (*) p < 0.001; (**) p < 0.02 by two-tailed Student’s t -test.
Article Snippet: Types of primary antibodies and the dilutions used for immunofluorescence were as follows: anti-γH2AX (Millipore Sigma, 05-636, 1:400); anti-p21 (Santa Cruz Biotechnology, sc-6246, 1:100); anti-phospho ATM [S1981] (Millipore Sigma, 05-740, 1:200);
Techniques: CRISPR, Staining, Transduction, Two Tailed Test, Marker
Journal: PLoS ONE
Article Title: Tumor-targeted SN38 inhibits growth of early stage non-small cell lung cancer (NSCLC) in a KRas/p53 transgenic mouse model
doi: 10.1371/journal.pone.0176747
Figure Lengend Snippet: A . Quantification of CellTiterBlue (CTB) viability assay in human A549 and H441 NSCLC cell lines treated with vehicle, STA-8666 and irinotecan in doses of 0.1, 1, 10 μM for up to 5 days. Chart curves represent average data from two independent runs performed with duplicate samples. B-E . Western blot analysis of phosphorylated (p) and total (t) ERK1/2 ( B ), AKT ( C ), CHK2 ( D ) and CDK1 ( E ) protein expression in human A549 and H441 NSCLC cell lines, at 48 hours after treatment with vehicle (V), STA-8666 and irinotecan in doses of 0.1, 1, or 10 μM, as indicated. Histograms represent data from two independent experiments. All graphs: *, p≤0.05; **, p≤0.01; ***, p≤0.001 relative to vehicle controls.
Article Snippet: Primary antibodies were used at a 1:1000 dilution and included: anti-PARP (#9542L Cell Signaling, Beverly, MA), anti-pT 202 /Y 204 -ERK1/2 (#4996S Cell Signaling, Beverly, MA), anti-Erk1/2, (#4696S Cell Signaling, Beverly, MA), anti-p T308 Akt, (#2965S Cell Signaling, Beverly, MA), anti-Akt, (#2920S Cell Signaling, Beverly, MA),
Techniques: Viability Assay, Western Blot, Expressing