S26A4 Polyclonal Antibody Sizes: 50μL, 100μL Catalogue Numbers: RA34657-50, RA34657-100 Citations, Manuals and MSDS Available upon request. Background: solute carrier family 26 member 4 (SLC26A4) Homo sapiens 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], Condition: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide. Storage Instructions: -20°C/1 year Recommended dilutions: WB 1:500-2000 ELISA 1:5000-20000 Applications: WB; ELISA Species Cross-Reactivity: Human; Rat; Mouse GeneID (Human): 5172 Protein MW (KDa): 85 SWISS: O43511 Source: Rabbit Research Use Only