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Histone antibody

The Mouse Monoclonal anti- antibody has been validated for WB, IHC (p), FACS and IF. It is suitable to detect in samples from Human, Rat and Mouse.
Catalog No. ABIN3024807

Quick Overview for Histone antibody (ABIN3024807)

Target

Histone

Reactivity

  • 16
  • 5
  • 5
  • 2
  • 1
  • 1
Human, Rat, Mouse

Host

  • 14
  • 5
  • 1
Mouse

Clonality

  • 15
  • 5
Monoclonal

Conjugate

  • 16
  • 4
Un-conjugated

Application

  • 19
  • 13
  • 8
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunofluorescence (IF)

Clone

AE-4
  • Purification

    Protein G affinity chromatography

    Immunogen

    Nuclei of human leukemia biopsy cells were used as the immunogen for the Histone antibody.

    Isotype

    IgG2a kappa
  • Application Notes

    Optimal dilution of the Histone antibody should be determined by the researcher.

    1. Staining of formalin/paraffin tissues requires boiling tissue sections in 10  mM Citrate buffer,  pH 6.0, for 10-20 min followed by cooling at RT for 20 min.
    2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.\. Western blot: 0.5-1 μg/mL, Flow Cytometry: 0.5-1 μg/million cells in 0.1ml,Immunofluorescence: 0.5-1 μg/mL,Immunohistochemistry (FFPE): 0.5-1 μg/mL for 30 min at RT (1),Prediluted format : incubate for 30 min at RT (2)

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

    Store the Histone antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide).
  • Target

    Histone

    Background

    Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer, formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80 % of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.
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