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EWSR1 antibody

The Rabbit Polyclonal anti-EWSR1 antibody has been validated for WB, ELISA and IHC. It is suitable to detect EWSR1 in samples from Human and Mouse.
Catalog No. ABIN7247048

Quick Overview for EWSR1 antibody (ABIN7247048)

Target

See all EWSR1 Antibodies
EWSR1 (Ewing Sarcoma Breakpoint Region 1 (EWSR1))

Reactivity

  • 72
  • 35
  • 30
  • 11
  • 8
  • 8
  • 7
  • 7
  • 6
  • 5
  • 5
  • 3
  • 2
  • 1
Human, Mouse

Host

  • 60
  • 10
  • 2
  • 1
Rabbit

Clonality

  • 62
  • 11
Polyclonal

Conjugate

  • 55
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EWSR1 antibody is un-conjugated

Application

  • 63
  • 27
  • 17
  • 15
  • 6
  • 5
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human EWSR1

    Isotype

    IgG
  • Application Notes

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.26 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    EWSR1 (Ewing Sarcoma Breakpoint Region 1 (EWSR1))

    Alternative Name

    EWSR1

    Background

    This gene encodes a multifunctional protein that is involved in various cellular processes, including gene expression, cell signaling, and RNA processing and transport. The protein includes an N-terminal transcriptional activation domain and a C-terminal RNA-binding domain. Chromosomal translocations between this gene and various genes encoding transcription factors result in the production of chimeric proteins that are involved in tumorigenesis. These chimeric proteins usually consist of the N-terminal transcriptional activation domain of this protein fused to the C-terminal DNA-binding domain of the transcription factor protein. Mutations in this gene, specifically a t(11,22)(q24,q12) translocation, are known to cause Ewing sarcoma as well as neuroectodermal and various other tumors. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and 14.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 68 kDa

    UniProt

    Q01844
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