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WFS1 Peptide

WFS1 Peptide

Cat no: BS60455P

Supplier: Bioworld Technology, Inc.
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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.
Catalogue number: BS60455P
Applications: Block/Neutralize/Inhibit
Swiss prot: O76024
Form: 1 mg/ml in DI water.
Purity: Synthetic peptide WFS1. (Note: the amino acid sequence is proprietary). The purity is > 98%.
Storage temp: Store at 4 degree C short term. Aliquot and store at -20 degree C long term. Avoid freeze-thaw cycles.
Alternative names: Wolframin
Additional info: This peptide can be used with studies using BS60455 WFS1 pAb.

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