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ATRX antibody (AA 2311-2492)

This anti-ATRX antibody is a Mouse Monoclonal antibody detecting ATRX in ELISA. Suitable for Human.
Catalog No. ABIN5611354

Quick Overview for ATRX antibody (AA 2311-2492) (ABIN5611354)

Target

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

Reactivity

  • 71
  • 17
  • 4
  • 3
  • 2
  • 2
Human

Host

  • 43
  • 30
  • 1
Mouse

Clonality

  • 42
  • 32
Monoclonal

Conjugate

  • 38
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ATRX antibody is un-conjugated

Application

  • 30
  • 27
  • 22
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  • 12
  • 11
  • 9
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
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  • 1
ELISA

Clone

8B2H9
  • Binding Specificity

    • 8
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2311-2492

    Purpose

    ATRX Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human ATRX (AA: 2311-2492) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 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. 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. Mutations in 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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.

    Molecular Weight

    282.5 kDa

    Gene ID

    546
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