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Image Search Results
Journal: PLoS ONE
Article Title: Temporal Association of Herpes Simplex Virus ICP4 with Cellular Complexes Functioning at Multiple Steps in PolII Transcription
doi: 10.1371/journal.pone.0078242
Figure Lengend Snippet: Novel complexes copurifying with ICP4 (spectral counts).
Article Snippet: The antibodies used to probe the membranes were; N15, polyclonal rabbit serum, for ICP4 (1:500), Trap220/Med 1 (sc-8998-X), Med6 (sc-9434), Med 4 (NBP1-84977; Novus Biologicals), Med23 (550429; BD Bio), CDK8 (sc-1521), Med12 (NB100-2357; Novus Biologicals), Med 13 ((NB100-60642; Novus Biologicals), Med 26 (sc-166614), TAF1 (sc735), TBP (233-R Covance), p62 (sc292-X), p80/XPB (sc-20696-x), CPSF2 (sc-165983),
Techniques:
Journal: PLoS ONE
Article Title: Temporal Association of Herpes Simplex Virus ICP4 with Cellular Complexes Functioning at Multiple Steps in PolII Transcription
doi: 10.1371/journal.pone.0078242
Figure Lengend Snippet: Western blot analysis of nuclear extracts (NE) or affinity purified (PD) samples collected at 6 hpi using either wtICP4 (KOS) or TAP-wtICP4 (TAP) expressing viruses. Antibodies directed against (A) p80 and p62 of TFIIH, (B) CPSF2 and CPSF7 of the cleavage and polyadenylation complex and (C) Brahma of Swi/Snf, CHD3 of the Nurd complex, and RuvBL1 and RuvBL2 of the Ino80 complex were used.
Article Snippet: The antibodies used to probe the membranes were; N15, polyclonal rabbit serum, for ICP4 (1:500), Trap220/Med 1 (sc-8998-X), Med6 (sc-9434), Med 4 (NBP1-84977; Novus Biologicals), Med23 (550429; BD Bio), CDK8 (sc-1521), Med12 (NB100-2357; Novus Biologicals), Med 13 ((NB100-60642; Novus Biologicals), Med 26 (sc-166614), TAF1 (sc735), TBP (233-R Covance), p62 (sc292-X), p80/XPB (sc-20696-x), CPSF2 (sc-165983),
Techniques: Western Blot, Affinity Purification, Expressing
Journal: Hepatology Communications
Article Title: Genome-wide CRISPR screen identifies ACSL3 as a regulator of lipotoxicity and progression of MASLD
doi: 10.1097/HC9.0000000000000884
Figure Lengend Snippet: ACSL3 loss confers resistance to palmitic acid–induced cell death. (A) Left, ACSL3 protein by western blot; right, viability of ACSL3-KO and NC HLF cells after 72 hours PA. (B) Left, INSIG1 protein by western blot; right, viability of INSIG1-KO and NC HLF cells after 72 hours PA. (C, D) Primary human hepatocytes (isolated from humanized mice) transfected with ACSL3 siRNA; ACSL3 mRNA by RT-qPCR normalized to ACTB (C), and PA-induced changes in viability and caspase-3/7 activity (D). (E) Real-time imaging (IncuCyte) of confluence in ACSL3-KO and NC HLF cells during day 1–6 PA exposure. (F) Viability of HLF cells treated with PA with or without the pan-ACSL inhibitor triacsin. (G) Flow-cytometric quantification of Annexin V and propidium iodide-positive cells after 24 hours PA in ACSL3-KO versus NC HLF cells. (H) ACSL3 and GRP78 mRNA by RT-qPCR normalized to ACTB following PA exposure. Abbreviations: ACSL3, acyl-CoA synthetase long-chain family member 3; KO, knockout; NC, negative control; PA, palmitic acid; siRNA, small interfering RNA; WT, wild type.
Article Snippet: Library preparation was performed in the Genomics Core (Institute of Microbiology) using the
Techniques: Western Blot, Isolation, Transfection, Quantitative RT-PCR, Activity Assay, Imaging, Knock-Out, Negative Control, Small Interfering RNA
Journal: Hepatology Communications
Article Title: Genome-wide CRISPR screen identifies ACSL3 as a regulator of lipotoxicity and progression of MASLD
doi: 10.1097/HC9.0000000000000884
Figure Lengend Snippet: ACSL3 deficiency abrogates PA-induced activation of lipogenic programs without enhancing β-oxidation. (A–C) mRNA levels by RT-qPCR normalized to ACTB: CPT1, CPT2, and ACOX (A); SCD, ChREBP, and SREBP1 (B); PPARG and LXRA (C). Abbreviations: KO, knockout; WT, wild type.
Article Snippet: Library preparation was performed in the Genomics Core (Institute of Microbiology) using the
Techniques: Activation Assay, Quantitative RT-PCR, Knock-Out