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Anti parp antibody

Manufactured by Cell Signaling Technology
Sourced in United States

The Anti-PARP antibody is a laboratory reagent used to detect and quantify the presence of PARP (Poly(ADP-Ribose) Polymerase) proteins in biological samples. PARP is an enzyme involved in various cellular processes, including DNA repair and programmed cell death. The Anti-PARP antibody can be used in techniques such as Western blotting, immunoprecipitation, and immunohistochemistry to identify and analyze PARP proteins.

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49 protocols using anti parp antibody

1

Antibody Identification and Characterization

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Mouse anti-tubulin (#05-829) was from Millipore (Darmstadt, Germany). For monoclonal mouse antibody C10 and polyclonal rabbit anti-human Ddx17 antibody, see [17 (link),19 (link)]. Mouse monoclonal anti-c-myc (clone 9E10) and rat anti-HA (clone 3F10) antibodies were purchased from Roche. Mouse anti-GFP (MAB3580) was from Upstate (New York, NY, USA). For monoclonal antibodies PAb101, see [50 (link)]. Rabbit polyclonal anti-HDAC1 was from Santa Cruz (Heidelberg, Germany). Rabbit monoclonal anti-histone H3 (D2B12XP, ChIP formulated) as well as anti-PARP antibodies were from Cell Signaling Technology (Frankfurt, Germany); horseradish peroxidase-conjugated goat anti-mouse (A4416) and goat anti-rabbit (A0545) antibodies were from Sigma (Taufkirchen, Germany).
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2

Immunofluorescence Profiling of Nephropathy

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Goat polyclonal anti‐nephrin N20, mouse monoclonal anti‐VDR (D‐6) and rabbit polyclonal anti‐RXR (C‐20) antibodies were purchased from Santa Cruz Biotechnology. Rabbit polyclonal anti‐PODXL antibody was purchased from Thermo Fisher Scientific (MA, USA). Rabbit monoclonal anti‐p85α/PI3 kinase antibody was purchased from Millipore (MA, USA). Rabbit polyclonal anti‐Akt, rabbit monoclonal anti‐phospho‐Ser473 Akt, rabbit polyclonal anti‐cleaved caspase‐3 and anti‐PARP antibodies were purchased from Cell Signaling. Mouse monoclonal anti‐tubulin antibody was purchased from Sigma‐Aldrich Ltd., (Gillingham, UK) Fluorescent secondary antibodies, donkey anti‐rabbit Alexa Fluor 594, donkey anti‐goat Alexa Fluor 488, donkey antimouse Alexa Fluor 594 and donkey antimouse Alexa Fluor 488 were purchased from Molecular Probes, Invitrogen Thermo Fisher Scientific, MA, USA. STZ was purchased from Sigma‐Aldrich.
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3

Cytokine-Induced Inflammatory Signaling

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The following reagents were purchased from the indicated manufacturers: rh IL-6 and TNFα were obtained from PEPROTECH (Rocky Hill, NJ, USA) and anti-P-STAT3, anti-STAT3, anti- NFκB p-p65, anti-NFκBp65, and anti-PARP antibodies were obtained from Cell Signaling Technology (Boston, MA, USA). Anti-GAPDH antibody was purchased from Santa Cruz Biotechnology (Dallas, TX, USA) and the anti-URI antibody was from Proteintech (Chicago, IL, USA). Bortezomib was purchased from Selleckchem (Houston, TX, USA).
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4

Adipocyte Differentiation Assay with 3T3-L1 Cells

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3T3-L1 cells (ATCC Cat. number CL-173) were purchased from the Bioresource Collection and Research Centre (Food Industry Research and Development Institute, Hsinchu, Taiwan). Anti-β-actin antibodies, 4,6-diamidino-2-phenylindole dihydrochloride (DAPI), dexamethasone (DEX), formaldehyde, insulin, 3-isobutyl-1-methylxanthine (IBMX), Oil Red O, propidium iodide (PI), and Triton X-100 were purchased from Sigma-Aldrich (Missouri, USA). Anti-caspase-3 and anti-PARP antibodies were purchased from Cell Signaling Technology (MA, USA). Fetal bovine serum (FBS) was purchased from Thermo Fisher Scientific Inc. (NY, USA). The PCR Amplification Kit was purchased from the Takara Bio Inc. (Shiga, Japan). Percoll was purchased from GE Healthcare Bio-Sciences AB (Uppsala, Sweden). Trypan blue solution (0.5%) was purchased from BioWest (Nuaille, France). All other reagents were purchased from Invitrogen (CA, USA).
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5

Apoptosis Signaling Pathway Evaluation

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Anti-Caspase-3, Anti-Caspase-8, Anti-Caspase-9, and anti-PARP antibodies for Western blotting were purchased from Cell Signaling Technology (Danvers, MA). Anti-Calreticulin antibody was purchased from Enzo Life Sciences (Farmingdale, NY). Anti-rabbit and anti-mouse HRP conjugated secondary antibodies were purchased from Cell Signaling Technology (Danvers, MA). For cell viability assays, Annexin V FITC/propidium iodide (BD Biosciences) was used following the protocol of the manufacturer.
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6

Western Blot Antibody Panel

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Anti-S6 ribosomal protein antibodies S6 and pS6, anti-mTOR (raptor and rictor) and anti-PARP antibodies were from Cell Signaling Technology. Anti-β-actin antibody was from Sigma. The goat anti-mouse IgG-HRP, goat anti-rabbit IgG-HRP, goat anti-mouse IgG-biotin and goat anti rabbit-IgG-biotin second antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Vectastain ABC kit and DAB substrate kit were from Vector Laboratories.
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7

Xenograft Mouse Model for AR-42 Treatment

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AR-42 was a kind gift from Arno Therapeutics, Inc. (Flemington, NJ). Stock solution of AR-42 (100 mM) was prepared in dimethyl sulfoxide (DMSO) (Sigma-Aldrich, St. Louis, MO) and stored at –20°C. For in vivo experiments, AR-42 was prepared as a suspension in a vehicle [10% DMSO, 0.5% methylcellulose (w/v), and 0.1% Tween 80 (v/v) in sterile water] for oral administration to xenograft-bearing athymic nude mice. Anti-cyclin B1 (GNS1), anti-cyclin B2 (H-105), anti-γH2AX, anti-survivin (D-8), anti-XIAP (A-7), anti-caspase 8, anti-apoptosis inducing factor (AIF) (E1), anti-mouse IgG-CFL 488, anti-p21 (C19), anti-E-cadherin (H108) and anti-p53 (DO-1) antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA) Anti-caspase 9 (C9), anti-caspase 3, and anti-PARP antibodies were from Cell Signaling Technologies (Beverly, MA). Anti-histone H4 antibody was purchased from Active Motif (Rixensart, Belgium). Anti-N-cadherin was from Genetex (GTX112733, GeneTex Inc., San Antonio, TX).
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8

Western Blot Analysis of Protein Targets

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Western blot was performed as described [41 (link)]. Antibodies against p53, p21, Egr-1, IRP2 (The anti-IRP2 antibody used in Figs. 35 and Fig. 6 have different lot number), FTH1, TfR1, and actin were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-mouse IRP2 antibody was a generous gift of Elizabeth Leibold (University of Utah) [53 (link)]. Anti-mouse p53 (1C12) and anti-PARP antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA). Antibodies against FDXR were purchased from Abcam (Cambridge, MA, USA). HRP-conjugated secondary antibodies against rabbit and mouse IgG were purchased from BioRad (Hercules, CA). The immunoreactive bands were visualized by enhanced chemiluminescence (Thermo Fisher Scientific Inc, Carlsbad, CA) and quantified by densitometry with the BioSpectrum® 810 Imaging System (UVP LLC, Upland, CA).
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9

Apoptosis-related Protein Expression Analysis

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Mouse anti-caspase-9, Bcl2, Bax, AKT, p-AKT and anti-PARP antibodies were from Cell Signaling Technology. mTOR, p- mTOR, PTEN, p-PTEN, p38, p-p38, CFLAR were from SANTA CRUZ. DR4 and DR5 were from Boster. Rabbit anti ISG12a antibody was from Abcam (ab171919). Mouse anti-β-actin and anti-V5 monoclonal antibody were from Sigma and Invitrogen respectively. Pancaspase inhibitor z-VAD-FMK was obtained from Promega. 2'-O-me-anti-miR-942 (5'-CACAUGGCCAAAACAGAGAAGA-3') & 2'-O-me-GFP miR (5'-AAGGCAAGCUGACCCUGAAGU-3') were from Takara. The Annexin V-FITC apoptosis detection kit and TRAIL were purchased from BD Pharmingen and R&D Systems respectively.
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10

Western Blot Antibody Validation

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The primary antibodies used for western blot analysis were polyclonal rabbit anti-human ISG15 antibodies (Abcam, Cambridge, MA, USA) and mouse anti-β-actin antibodies (Sigma, St Louis, MO, USA). Anti-PARP antibodies were obtained from Cell Signaling Technology (Danvers, MA, USA) and TRAIL from BD Pharmingen (San Diego, CA, USA).
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