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H2AFX antibody (pSer139)

This anti-H2AFX antibody is a Mouse Monoclonal antibody detecting H2AFX in WB and ICC. Suitable for Human and Mouse.
Catalog No. ABIN6241012

Quick Overview for H2AFX antibody (pSer139) (ABIN6241012)

Target

See all H2AFX Antibodies
H2AFX (H2A Histone Family, Member X (H2AFX))

Reactivity

  • 170
  • 82
  • 61
  • 25
  • 25
  • 19
  • 17
  • 11
  • 8
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 156
  • 17
  • 2
Mouse

Clonality

  • 127
  • 48
Monoclonal

Conjugate

  • 119
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
This H2AFX antibody is un-conjugated

Application

  • 137
  • 57
  • 49
  • 44
  • 33
  • 28
  • 27
  • 21
  • 16
  • 15
  • 8
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunocytochemistry (ICC)
  • Binding Specificity

    • 35
    • 20
    • 18
    • 11
    • 6
    • 5
    • 5
    • 5
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer139

    Immunogen

    Recombinant Protein
  • Application Notes

    WB: 1:2000. ICC: 1:400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Storage

    4 °C,-20 °C
  • Target

    H2AFX (H2A Histone Family, Member X (H2AFX))

    Alternative Name

    Histone H2A.X

    Background

    Variant histone H2A which replaces conventional H2A in a subset of nucleosomes. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. Required for checkpoint-mediated arrest of cell cycle progression in response to low doses of ionizing radiation and for efficient repair of DNA double strand breaks (DSBs) specifically when modified by C- terminal phosphorylation.

    UniProt

    P16104

    Pathways

    Telomere Maintenance, DNA Damage Repair, Positive Regulation of Response to DNA Damage Stimulus
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