
Sku: WP7100
Catalog No.: WP3247
Specification: 50μL/100μL
Stock: In stock
U-Blot® S26A4 Polyclonal Antibody Learn more
Background:Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008],
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