| Product Name | S26A4 Polyclonal Antibody |
| Cat Number | HR1AP12925 |
| Source | Rabbit |
| Applications | WB,ELISA |
| Species Reactivity | Human |
| Storage | -20°C/1 year |
| Purification | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| Concentration | 1 mg/ml |
| Observed Band | 85 |
| Gene ID | SLC26A4 PDS |
| 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], |
| Type | polyclonal |