Rabbit
WB,ELISA
Human,Mouse
WB 1:500-2000 ELISA 1:5000-20000
-20°C/1 year
WFS1 Polyclonal Antibody detects endogenous levels of protein.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Synthesized peptide derived from part region of human protein
O76024
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Polyclonal
IgG
wolframin ER transmembrane glycoprotein(WFS1) Homo sapiens 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],
WFS1, Wolframin
1 mg/ml
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