• Product NameSLC26A4 Polyclonal Antibody
• Host SpeciesRabbit
• ClonalityPolyclonal
• IsotypeIgG
• PurificationAffinity purification
• ApplicationsWB
• Species ReactivityMouse
• Immunogen DescriptionA synthetic peptide of human SLC26A4 (NP_000432.1).
• Alternative Names    SLC26A4; DFNB4; EVA; PDS; TDH2B; pendrin
• Accession No. Swiss-Prot#:O43511
  NCBI Gene ID:5172
• UniprotO43511
• Gene ID5172;
• Calculated MW 86kDa
• Formulation Avoid freeze / thaw cycles.|Buffer: PBS with 50% glycerol, pH7.4.
• Storage Store at -20˚C

• WB 1:500 - 1:2000

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.

• Western blot analysis of extracts of mouse liver, using SLC26A4 at 1:1000 dilution.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting