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Anti histone h3 antibody

Manufactured by Proteintech
Sourced in China

The Anti-Histone H3 antibody is a primary antibody used for the detection and analysis of histone H3 in various applications, such as Western blotting, immunoprecipitation, and immunocytochemistry. Histone H3 is a core histone protein that plays a crucial role in the organization and regulation of chromatin structure within the cell nucleus.

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4 protocols using anti histone h3 antibody

1

Polysaccharide Extraction and Characterization from Annona squamosa

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A. squamosa was purchased from Guangzhou Tianhe fruit wholesale market, Guangzhou, China. The pulp material was identified by Professor R.M. Yu, College of Pharmacy, Jinan University, China. Standard monosaccharides and T-series dextrans were obtained from Sigma Chemical Co. (St. Louis, MO, USA). DEAE-52 cellulose and Sephadex G-100 were obtained from Whatman Ltd (Kent County, England). Sephacryl S-300 HR was obtained from Amersham Biosciences (Pharmacia, Uppsala, Sweden). The rmGM-CSF (214-14) and rmIL-4 (315-03) were obtained from PeproTechInc (Rocky Hill, NJ, USA). Anti-CD11c-FITC, anti-MHC II-PE, anti-CD86-FITC and anti-CD11c-APC antibodies were purchased from eBioscience (San Diego, CA, USA). Neutral red was purchased from Amresco (Albany, NY, USA) and the NO assay kit was supplied by the Beyotime Institute of Biotechnology (Haimen, China). Lipopolysaccharide (LPS) and FITC-dextran were purchased from Sigma–Aldrich (St. Louis, MO, USA). Anti-β-actin and anti-GAPDH antibodies were obtained from Biosharp (Beijing, China). Anti-Histone-H3 antibody was obtained from Proteintech (Wuhan, China). MAPK family antibody sampler kit and NF-κB pathway sampler kit were purchased from Cell Signaling Technology (Beverly, MA, USA). Other chemicals and reagents were of analytical grade.
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2

Western Blot Technique for Protein Analysis

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Cells were collected and lysed with RIPA lysis buffer (Beyotime, P0013B). The protein concentrations were evaluated via Enhanced BCA Protein Assay Kit (Beyotime). Protein lysates were separated by electrophoresis on a sodium dodecyl sulfate‐polyacrylamide gel (8%‐15%), transferred onto PVDF membranes, and incubated with primary antibodies at 4°C overnight followed by goat anti‐rabbit or goat anti‐mouse IgG (Proteintech) at 37°C for 40 minutes. The protein bands were visualized by enhanced chemiluminescence (ECL). Primary antibodies used in this study were as follows: anti‐δ‐Catenin antibody (Bioss, bs‐22251R), anti‐Cyclin D1 antibody (CST, #2922), anti‐CDK6 antibody (Proteintech, 19117‐1‐AP), anti‐CDK4 antibody (CST, #12790), anti‐c‐myc antibody (Proteintech, 10828‐1‐AP), anti‐Bcl2L1 antibody (Proteintech, 10783‐1‐AP), anti‐cleaved‐caspase‐3 antibody (CST, #9661), anti‐survivin antibody (Proteintech, 10508‐1‐AP), anti‐β‐catenin antibody (CST, #8480), anti‐β‐actin antibody (Proteintech, 60008‐1‐Ig), anti‐Histone H3 antibody (Proteintech, 17168‐1‐AP).
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3

Comprehensive Antibody Validation Protocol

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The following primary antibodies were used in our experiments: anti‐GAPDH antibody (Proteintech), anti‐Histone H3 antibody (Proteintech), anti‐phospho‐p70S6K antibody (T389) (Cell Signaling Technology), anti‐p70S6K antibody (Epitomics), anti‐LAMP1 antibody (Abcam), anti‐LAMP2 antibody (Santa Cruz), anti‐TFEB antibody (Cell Signaling Technology), anti‐p62 antibody (Enzo Life Sciences), anti‐mTOR antibody (Cell Signaling Technology), anti‐HA antibody (Santa Cruz), anti‐FLAG antibody (Sigma), anti‐GFP antibody (Santa Cruz), anti‐Rag B antibody (Cell Signaling Technology), anti‐raptor antibody (Cell Signaling Technology), anti‐α‐Tubulin (Proteintech), and anti‐C9orf72 (Santa Cruz). The following secondary antibodies were used: horseradish peroxidase‐conjugated sheep anti‐mouse and anti‐rabbit antibodies (Jackson ImmunoResearch Laboratories). The following fluorescent secondary antibodies were used: Alexa Fluor 594‐conjugated goat anti‐rabbit IgG (Proteintech), Alexa Fluor 594‐conjugated goat anti‐mouse IgG (Proteintech), Alexa Fluor 488‐conjugated goat anti‐rabbit IgG (Proteintech), Alexa Fluor 488‐conjugated Goat anti‐mouse IgG (Proteintech), Alexa Fluor 660‐conjugated goat anti‐mouse IgG (H + L) highly cross‐adsorbed antibody (Invitrogen), and Alexa Fluor 405‐conjugated goat anti‐rabbit IgG (H + L) secondary antibody (Invitrogen).
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4

Antibody Reagents for Protein Analysis

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Anti-NCOA3 antibody (#2126), anti-SP1 (D4C3) antibody (#9389), and anti-Acetylated-Lysine antibody (#9441) were purchased from Cell Signaling Technology (Danvers, MA). Anti-TERT antibody (#NB110-89471) was from Novus Biologicals (Littleton, CO). Anti-NCOA3 ChIP grade antibody (#ab2782) was from Abcam (Cambridge, MA). Anti-GAPDH antibody (#10494-1-AP), anti-histone H3 antibody (#17168-1-AP), horseradish peroxidase (HRP)-conjugated Goat Anti-Rabbit IgG antibody (#SA00001-2), Alexa Fluor 488 conjugated Goat Anti-Mouse IgG antibody (#SA00006-1), Alexa Fluor 594 conjugated Goat Anti-Rabbit IgG antibody (#SA00006-4) were from Proteintech (Wuhan, China). Real-time quantitative polymerase chain reaction (qPCR) reagents (#QPK-201) were from TOYOBO (Shanghai, China). A dual-luciferase detection kit (E1910) was obtained from Promega (Madison, WI).
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