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Home / Antibodies

Anti-WFS1 Antibody BHA11303593

SKU : BHA11303593

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Mfr.No.	BS60455
Alternative Names	Wolframin
Categories	Primary Antibodies
Chromosome Location	4p16.1
Clonality	polyclonal
Description	The Wolframin gene encodes a protein found in endoplasmic reticulum membrane of several tissues including brain, pancreas, lung and placenta. Loss-of-function mutations in both alleles result in Wolfram syndrome (also known as DIDMOAD, an autosomal recessive disorder that causes juvenile diabetes mellitus, diabetes insipidus, optic atrophy and a number of neurological symptoms including deafness, ataxia and peripheral neuropathy. A large number and variety of mutations in this gene, particularly in exon 8, can be associated with Wolfram syndrome. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38.
Host	Rabbit
Immunogen	A synthetic peptide corresponding to residues in Human WFS1.
Reactivity	Human, Mouse, Rat
Recombinant	FALSE
Regulatory	RUO
Species	Homo Sapiens (Human)

Swissprot	O76024
Uniprot	O76024
Weight	100 kDa

Description	Product: 1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol. Specificity: WFS1 polyclonal antibody detects endogenous levels of WFS1 protein.
Purity	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Applications

WB

Description

WB

Dilution

WB	1:500-1:1000

Datasheet

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SKU	Supplier No.	Size	Your price	Quantity
BHA11303593	BS60455	50µl	$190.44		Add to Cart
BHA11303593	BS60455	100µl	$294.44		Add to Cart

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