Tissue expression
Cell line expression
Protein structure

WFS1

Wolframin ER transmembrane glycoprotein
DFNA14, DFNA38, DFNA6, DIDMOAD, WFS 
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]
More gene data

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204 antibodies from 27 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Proteintech Group
3 antibodies
Boster Biological Technology
2 antibodies
Biorbyt
38 antibodies
NovoPro Bioscience Inc.
2 antibodies
Abnova Corporation
2 antibodies
Wuhan Fine Biotech Co., Ltd.
1 antibody
antibodies-online
56 antibodies
St John's Laboratory
2 antibodies
Affinity Biosciences
1 antibody
Cusabio Biotech Co., Ltd
1 antibody
Invitrogen Antibodies
7 antibodies
Bioworld Technology, Inc
3 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Cell Signaling Technology, Inc
1 antibody
Novus Biologicals
2 antibodies
GeneTex
2 antibodies
Atlas Antibodies
1 antibody
R&D Systems
1 antibody
Creative Biolabs
3 antibodies
United States Biological
36 antibodies
Creative Diagnostics
4 antibodies
MyBioSource
2 antibodies
Leading Biology
1 antibody
Abbexa
2 antibodies
MilliporeSigma / Merck KGaA
1 antibody