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2 protocols using anti actin hrp conjugated

1

Western Blot Analysis of Cell Signaling

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Samples were treated with lysis buffer [Tris–HCl 50mM pH7.4, 10% NP-40, 0.25% NaDesoxycholate, EDTA 1mM, NaCl 150mM, PMSF 1mM, protease inhibitor cocktail (Roche)] and loaded onto pre-cast 4–12% gradient acrylamide gels (NuPAGE, Invitrogen). After electro-blotting, filters were incubated with anti-AKTIP (Sigma), anti-TRF2 (Novus Biologicals), anti-actin-HRP conjugated (Santa Cruz), anti-cyclin A (Santa Cruz), anti-cyclin B (Santa Cruz), anti-cyclin E (Upstate Biotechnology), anti-p53-pSer15 (Cell Signaling Technology), anti-p53 (DakoCytomation), anti-ATM-pS1981 (Rockland Immunochemicals), anti-ATM (Genetex), anti-ChK1-PSer345 (Cell Signaling Technology), anti-AKT (Cell Signaling Technology), anti-PCNA (Santa Cruz), anti-RPA70 (Santa Cruz), or anti-TRF1 (Santa Cruz). Filters were then incubated with appropriate HRP-conjugated secondary antibodies (Santa Cruz), which were detected using the enhanced chemiluminescence system (ECL plus, Amersham). Signals were quantified with Image J software.
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2

Western Blot Analysis of DNA Damage Response

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Cells were harvested and centrifuged at 5000 rpm for 5 min at 4 °C. The supernatant was removed, Buffer WCE 2X (100 mM TrisHCl pH 6.8, 4% SDS, 200 mM DTT) was added to resuspend the cell pellet, boiled for 10 min and then added an equal volume of SDS-PAGE Sample Loading Buffer [2X] (100 mM TrisHCl pH 6.8, 4% SDS, 200 mM DTT, 20% glycerol, 0.004% bromphenol blue) to the mixture. Cell extracts were pelleted at 15,000 g in an Eppendorf centrifuge for 15 min at 4 °C and the supernatants were analyzed by Western blotting according to [55 (link)], using the following antibodies, all diluted in TBS-T: anti-p-p53 (Ser 15; 1:1000, Santa Cell Signaling), anti-p53 (1:1000, Santa Cruz), anti-p-H2AX (Ser 139; 1:1000, Millipore), anti-SUV39H1 (44.1; 1:1000, Santa Cruz Biotechnology), anti-TDP-43 (1:5000, Proteintech), anti-H3k9me3 (1:1000, Abcam ab8898), anti-H3K9me2 (1:500, Abcam ab1220), anti-actin-HRP-conjugated (1:5000, Santa Cruz Biotechnology). These primary antibodies were detected using HRP conjugated anti-mouse and anti-rabbit IgGs and the ECL detection kit (all from GE Healthcare). Band intensities were quantified by densitometric analysis with Image Lab software (Bio-Rad).
All full length uncropped original western blots are available in the Supplementary Materials section.
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