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FUS antibody

This Rabbit Polyclonal antibody specifically detects FUS in IHC and ELISA. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7244078
-15% Promotion 2026
$457.98
$538.80
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Quick Overview for FUS antibody (ABIN7244078)

Target

See all FUS Antibodies
FUS (Fused in Sarcoma (FUS))

Reactivity

  • 67
  • 53
  • 45
  • 6
  • 6
  • 6
  • 4
  • 1
  • 1
Human, Mouse

Host

  • 84
  • 2
  • 1
Rabbit

Clonality

  • 66
  • 21
Polyclonal

Conjugate

  • 37
  • 7
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FUS antibody is un-conjugated

Application

  • 69
  • 41
  • 28
  • 23
  • 21
  • 16
  • 15
  • 14
  • 13
  • 12
  • 4
  • 3
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Fusion protein of human FUS

    Isotype

    IgG
  • Application Notes

    IHC 1:30-150, ELISA 1:2000-10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.7 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    FUS (Fused in Sarcoma (FUS))

    Alternative Name

    FUS

    Background

    This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6.

    UniProt

    P35637
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