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WFS1 antibody (AA 61-313)

The Rabbit Polyclonal anti-WFS1 antibody is suitable to detect WFS1 in samples from Human and Monkey. It has been validated for WB, ELISA, IF, IHC (p) and FACS.
Catalog No. ABIN7876107
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for WFS1 antibody (AA 61-313) (ABIN7876107)

Target

See all WFS1 Antibodies
WFS1 (Wolfram Syndrome 1 (WFS1))

Reactivity

  • 39
  • 8
  • 5
  • 2
Human, Monkey

Host

  • 36
  • 4
Rabbit

Clonality

  • 36
  • 4
Polyclonal

Conjugate

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This WFS1 antibody is un-conjugated

Application

  • 33
  • 13
  • 13
  • 13
  • 9
  • 5
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 61-313

    Purpose

    Wolframin Antibody / WFS1

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids A61-H313) was used as the immunogen for the Wolframin antibody.

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Wolframin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    WFS1 (Wolfram Syndrome 1 (WFS1))

    Alternative Name

    Wolframin

    Background

    Wolframin is a protein that in humans is encoded by the WFS1 gene. This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene.

    UniProt

    O76024

    Pathways

    Sensory Perception of Sound, Carbohydrate Homeostasis, ER-Nucleus Signaling, Negative Regulation of intrinsic apoptotic Signaling, SARS-CoV-2 Protein Interactome
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