SLC26A4 / Unconjugated / RB53308
Product Details
| Description | SLC26A4 Antibody - C-terminal region (OAAB22131) Unconjugated Rabbit Polyclonal Antibody, Reacts with Human, Mouse | |
|---|---|---|
| Conjugate | Unconjugated | |
| Clone | RB53308 | |
| Target Species | Human, Mouse | |
| Applications | WB | |
| Supplier | Aviva Systems Biology | |
| Catalog # | Sign in to view product details, citations, and spectra | |
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About SLC26A4
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]
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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