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WFS1 antibody

The Rabbit Polyclonal anti-WFS1 antibody is suitable to detect WFS1 in samples from Human and Mouse. It has been validated for WB and ELISA.
Catalog No. ABIN8125758
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for WFS1 antibody (ABIN8125758)

Target

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

Reactivity

  • 61
  • 14
  • 7
  • 4
Human, Mouse

Host

  • 58
  • 4
Rabbit

Clonality

  • 58
  • 4
Polyclonal

Conjugate

  • 22
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This WFS1 antibody is un-conjugated

Application

  • 55
  • 32
  • 20
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  • 5
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  • 3
  • 1
Western Blotting (WB), ELISA
  • Purpose

    WFS1 Antibody

    Specificity

    WFS1 Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from part region of human protein

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % 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

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    WFS1 (Wolfram Syndrome 1 (WFS1))

    Alternative Name

    WFS1

    Background

    Background: 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. [provided by RefSeq, Mar 2009],

    Gene Name: WFS1

    Protein Name: Wolframin

    Gene ID

    7466

    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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