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IHC-P analysis of postnatal mouse (PN19) lung sections using GTX80694 Histone H2A.XS139ph (phospho Ser139) antibody [3F2]. Increased staining intensity was observed in a genetic mouse model with DNA damage in airway cells. Antigen retrieval : heat induced epitope retrieval (HIER) method with sodium citrate buffer (pH 6.0) Fixation : 4% Paraformaldehyde Dilution : 1:400
IHC-P analysis of postnatal mouse (PN19) lung sections using GTX80694 Histone H2A.XS139ph (phospho Ser139) antibody [3F2]. Increased staining intensity was observed in a genetic mouse model with DNA damage in airway cells. Antigen retrieval : heat induced epitope retrieval (HIER) method with sodium citrate buffer (pH 6.0) Fixation : 4% Paraformaldehyde Dilution : 1:400
IHC-P analysis of postnatal mouse (PN19) lung sections using GTX80694 Histone H2A.XS139ph (phospho Ser139) antibody [3F2]. Increased staining intensity was observed in a genetic mouse model with DNA damage in airway cells. Antigen retrieval : heat induced epitope retrieval (HIER) method with sodium citrate buffer (pH 6.0) Fixation : 4% Paraformaldehyde Dilution : 1:400

Histone H2A.XS139ph (phospho Ser139) antibody [3F2]

GTX80694
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetH2AX
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Overview

  • Supplier
    GeneTex
  • Product Name
    Histone H2A.XS139ph (phospho Ser139) antibody [3F2]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 microg/ml. ICC/IF: 2-4 microg/ml. IHC-P: 1:400. FACS: 1microg per 106 cells. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    3F2
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3014
  • Target name
    H2AX
  • Target description
    H2A.X variant histone
  • Target synonyms
    H2A.X, H2A/X, H2AFX, histone H2AX, H2A histone family member X, H2AX histone, histone H2A.x
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP16104
  • Protein Name
    Histone H2AX
  • Scientific Description
    Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the histone H2A family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif. [provided by RefSeq, Oct 2015]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

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  • Wang YY, Chen YK, Hsu YL, et al. Synthetic β-nitrostyrene derivative CYT-Rx20 as inhibitor of oral cancer cell proliferation and tumor growth through glutathione suppression and reactive oxygen species induction. Head Neck. 2017,39(6):1055-1064. doi: 10.1002/hed.24664
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  • Shang HS, Chang CH, Chou YR, et al. Curcumin causes DNA damage and affects associated protein expression in HeLa human cervical cancer cells. Oncol Rep. 2016,36(4):2207-15. doi: 10.3892/or.2016.5002
    Read this paper
  • Lee JH, Guo Z, Myler LR, et al. Direct activation of ATM by resveratrol under oxidizing conditions. PLoS One. 2014,9(6):e97969. doi: 10.1371/journal.pone.0097969
    Read this paper
  • Smith S, Fox J, Mejia M, et al. Histone deacetylase inhibitors selectively target homology dependent DNA repair defective cells and elevate non-homologous endjoining activity. PLoS One. 2014,9(1):e87203. doi: 10.1371/journal.pone.0087203
    Read this paper
  • Fox JT, Sakamuru S, Huang R, et al. High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death. Proc Natl Acad Sci U S A. 2012,109(14):5423-8. doi: 10.1073/pnas.1114278109
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  • Kinjo T, Ham-Terhune J, Peloponese JM Jr, et al. Induction of reactive oxygen species by human T-cell leukemia virus type 1 tax correlates with DNA damage and expression of cellular senescence marker. J Virol. 2010,84(10):5431-7. doi: 10.1128/JVI.02460-09
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