SLC26A4 Polyclonal / Unconjugated /
Product Details
| Description | Specificity of human SLC26A4 antibody verified on a Protein Array containing target protein plus 383 other non-specific proteins. | |
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| Conjugate | Unconjugated | |
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| Target Species | Human | |
| Applications | IHC-P, IHC-Fr, IHC | |
| Supplier | Novus Biologicals | |
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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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115 SLC26A4 antibodies from over 13 suppliers available with over 26 conjugates.
