Phospho-gamma H2AX pSer139 Antibody Product Specific Information General Information PA1-25001 detects gamma H2A.X (phospho S139) from human and mouse samples. PA1-25001 has been successfully used in Immunoflourescence, and Western blot procedures. By Western Blot a band of ~15 kDa is detected.

Phosphorylated histone H2AX (γ-H2AX) is a potential regulator of DNA repair and is a (b) Representative data of western blotting for γ-H2AX in liver tissues.

Supplied as 100 µg purified antibody (1 mg/mL). Detection of human gamma-H2AX by western blot. Samples: Whole cell lysate (15 µg) from Jurkat cells treated with 100 µM etoposide for 4 hours (+) or mock treated (-). Antibody: Affinity purified rabbit anti-gamma-H2AX antibody A300-081A (lot A300-081A-19) used for WB at 0.1 µg/ml. Detection: Chemiluminescence with an exposure time of 10 seconds. Western blot - Anti-gamma H2A.X (phospho S139) antibody (ab2893) HeLa (Human epithelial cell line from cervix adenocarcinoma) cells were incubated at 37°C for 3h with vehicle control (0 µM) and different concentrations of camptothecin ( ab120115 ). Western blot - Anti-gamma H2A.X (phospho S139) antibody (ab11174) All lanes : Anti-gamma H2A.X (phospho S139) antibody (ab11174) at 0.04 µg/ml Lane 1 : Jurkat (human T cell leukemia cell line from peripheral blood) cells treated with 100 µM etoposide, whole cell lysate I have gotten good results with H2A.X and gH2A.X blots using antibodies from Cell Signaling.

View All Images (12) FC experiment of HepG2 using 10856-1-AP 1X10^6 HepG2 cells were stained with 0.2ug Histone H2A.X antibody (10856-1-AP, red) and control antibody (blue). While methods such as western blots and immunohistochemistry are widely used but difficult to validate to regulatory standards, the ELISA method is the most quantifiable and easiest to validate. To address this need Trevigen’s quantitative pharmacodynamic HT -H2AX assay measures -H2AX levels in cellular extracts Anti-phospho-Histone H2A.X (Ser139), clone 6L16 ZooMAb, is a recombinant Rabbit Monoclonal Antibody that specifically targets phospho Histone H2AX (ser139) and has been tested for use in Immunocytochemistry, Immunohistochemistry (Paraffin), Peptide Inhibition Assay, and Western Blotting. Bethyl Laboratories Anti-Phospho-gamma-H2AX (Ser139) Polyclonal, Catalog # A300-081A. Tested in Western Blot (WB), Immunofluorescence (IF), Immunocytochemistry (ICC) and Immunohistochemistry (IHC) applications. This antibody reacts with Human, Mouse samples. Supplied as 100 µL purified antibody (1 mg/mL).

Jose Joao Mansure, PhD, CCRP Research Associate, Research Institute, McGill University jose.mansure@mail.mcgill.ca Histone H2AX is a 14 kDa ubiquitous member of the H2A histone family that contains an evolutionarily conserved SQ motif at the C-terminus in eukaryotes. Serine 139 within this motif becomes rapidly phosphorylated by ATM and ATR Histone H2AX: Products.

Histone H2AX is a 14 kDa ubiquitous member of the H2A histone family that contains an evolutionarily conserved SQ motif at the C-terminus in eukaryotes. Serine 139 within this motif becomes rapidly phosphorylated by ATM and ATR

Expect a band approximately 15 kDa in size corresponding to phosphorylated H2AX protein by western blotting in the appropriate stimulated tissue or cell lysate or extract. 754 gamma H2AX antibodies from 38 antibody suppliers Click each gamma H2AX antibody that interests you to view the full gamma H2AX antibody datasheet Western Blot 2013-11-01 · Gamma-H2AX dephosphorylation by protein phosphatase 2A facilitates DNA double-strand break repair Mol. Cell , 20 ( 2005 ) , pp. 801 - 809 Article Download PDF View Record in Scopus Google Scholar Ainsi, H2AX contribue à la formation des nucléosomes et, par conséquent, à la structure de l'ADN. H2AX est phosphorylée au niveau de la sérine 139, appelé alors gamma-H2AX, en réaction aux coupures double-brin de l'ADN.

Western blot - Anti-gamma H2A.X (phospho S139) antibody (ab11174) All lanes : Anti-gamma H2A.X (phospho S139) antibody (ab11174) at 0.04 µg/ml Lane 1 : Jurkat (human T cell leukemia cell line from peripheral blood) cells treated with 100 µM etoposide, whole cell lysate

Serine 139 within this motif becomes rapidly phosphorylated by ATM and ATR Histone H2AX: Products. Histone H2AX is one of a number of core histone proteins. In the cellular response to genotoxic insults, ATM and related protein kinases phosphorylate the carboxyl-terminal tail of the H2AX protein (gamma-H2AX). gamma-H2AX marks the site of damage and provides a nucleation site for the formation of damage response and repair complexes. MA1-2022 detects human and mouse phosphorylated H2AX. MA1-2022 has been used successfully in Western blot, immunofluorescence, and ELISA procedures. By Western blot this antibody detects ~17 kDa protein representing phosphorylated H2AX in gamma irradiated HeLa cell lysate.

Histones play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA is wrapped around histone-groups, consisting of the core histones H2A, H2B, H3 and H4. As a reaction on DNA Double-strand breaks (DSB) H2AX becomes phosphorylated on serine 139, called gamma-H2AX. MA1-2022 detects human and mouse phosphorylated H2AX. MA1-2022 has been used successfully in Western blot, immunofluorescence, and ELISA procedures. By Western blot this antibody detects ~17 kDa protein representing phosphorylated H2AX in gamma irradiated HeLa cell lysate. Analysis of radiation-induced gamma-H2AX phosphorylation by western blot Molecular and Clinical Radiobiology Workshop McGill University Health Centre, June 17-19, 2015 ! Jose Joao Mansure, PhD, CCRP Research Associate, Research Institute, McGill University jose.mansure@mail.mcgill.ca Anti-phospho-Histone H2A.X (Ser139), clone 6L16 ZooMAb, is a recombinant Rabbit Monoclonal Antibody that specifically targets phospho Histone H2AX (ser139) and has been tested for use in Immunocytochemistry, Immunohistochemistry (Paraffin), Peptide Inhibition Assay, and Western Blotting.
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Using ionising radiation, we explored the kinetics of DNA lesion signaling and structural chromosome aberration formation at the intra- and inter-chromosomal level.

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Numb-IP effektivitet utvärderades av Western blot ( d ) och NICD-bindning till av Ki67 eller fosforylerad gamma H2AX histon (yH2AX) i MAoEC behandlade

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