S26A4 Polyclonal Antibody - BT-AP14005

S26A4 Polyclonal Antibody

Sizes: 20μL, 50μL, 100μL

Catalogue Numbers: BT-AP14005-20, BT-AP14005-50, BT-AP14005-100

Citations, Manuals and MSDS Available upon request.

Background: 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 3andapos; of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.

Research Areas: Signal transduction; Metabolism; Neuroscience

Target Protein: SLC26A4

Applications: WB, ELISA

Reactivity: Human, Rat, Mouse

Clonality: Polyclonal

Host: Rabbit

Isotype: IgG

Full Product Name: Pendrin

Immunogen: The antiserum was produced against synthesized peptide derived from human AMPK alpha around the phosphorylation site of Thr172. AA range:140-189

Storage: -20°C for 1 year

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Formulation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration: 1 mg/ml

UniProt Accession: Human: O43511; Mouse: Q9R155; Rat: Q9R154

Synonyms: Pendrin;Sodium-independent chloride/iodide transporter;Solute carrier family 26 member 4

GeneID: Human: 5172

Research Use Only