Recombinant Human SLC26A4 protein, MYC/DDK-tagged

• Cat.No.: SLC26A4-318H
• Product Overview: Recombinant Human SLC26A4 fused with MYC/DDK tag at C-terminal was expressed in HEK293.

Specification

• Description: 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.
• Source: HEK293
• Species: Human
• Tag: Myc&DDK
• Form: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
• Molecular Mass: 85.5 kDa
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Notes: Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
• Concentration: >50 ug/mL as determined by microplate BCA method

Gene Information

• Gene Name: SLC26A4 solute carrier family 26, member 4 [ Homo sapiens ]
• Official Symbol: SLC26A4
• Synonyms: SLC26A4; solute carrier family 26, member 4; DFNB4; pendrin; PDS; sodium-independent chloride/iodide transporter; EVA; TDH2B
• Gene ID: 5172
• mRNA Refseq: NM_000441
• Protein Refseq: NP_000432
• MIM: 605646
• UniProt ID: O43511
• Chromosome Location: 7q31
• Pathway: Multifunctional anion exchangers, organism-specific biosystem; SLC-mediated transmembrane transport, organism-specific biosystem; Transmembrane transport of small molecules, organism-specific biosystem; Transport of inorganic cations/anions and amino acids/oligopeptides, organism-specific biosystem
• Function: chloride transmembrane transporter activity; iodide transmembrane transporter activity; secondary active sulfate transmembrane transporter activity; sulfate transmembrane transporter activity; transporter activity