S26A4 Polyclonal Antibody Sizes: 50μL, 100μL Catalogue Numbers: RA34657-50, RA34657-100 Lead times: 1-2 weeks, if manufacturer has product in stock Manufacturer/Ship Location: China 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], Reactivity: Human, Rat, Mouse Host: Rabbit Applications: WB, ELISA Clonality: Polyclonal Dilution: WB 1:500-2000 ELISA 1:5000-20000 Molecular Weight: 85 Protein Molecular Weight (kDa): 85 Storage: -20°C/1 year Human Gene ID: 5172 Human SwissProt Number: O43511 Condition: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide. Research Use Only