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ATRX antibody (AA 2161-2413)

This anti-ATRX antibody is a Rabbit Polyclonal antibody detecting ATRX in WB, IHC and IF. Suitable for Human and Mouse.
Catalog No. ABIN1886208

Quick Overview for ATRX antibody (AA 2161-2413) (ABIN1886208)

Target

See all ATRX Antibodies
ATRX (helicase 2, X-linked (ATRX))

Reactivity

  • 73
  • 16
  • 4
  • 3
  • 2
  • 2
Human, Mouse

Host

  • 43
  • 32
  • 1
Rabbit

Clonality

  • 46
  • 30
Polyclonal

Conjugate

  • 39
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  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ATRX antibody is un-conjugated

Application

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  • 8
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  • 3
  • 3
  • 2
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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 8
    • 6
    • 3
    • 3
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    AA 2161-2413

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 2161 and 2413 of ATRX
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.250
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    ATRX (helicase 2, X-linked (ATRX))

    Alternative Name

    ATRX

    Background

    The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins.The mutations of this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome.These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes.This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis.Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.[provided by RefSeq]

    Molecular Weight

    283 kDa

    Gene ID

    546

    NCBI Accession

    NM_000489, NP_000480
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