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FIGURE: 1 / 2
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total SLC26A4.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: iodide/chloride transporter; Pendred syndrome homolog; sodium-independent chloride/iodide transporter; solute carrier family 26 (anion exchanger), member 4; unnamed protein product
Gene Aliases: DFNB4; EVA; PDS; pendrin; TDH2B
UniProt ID: (Human) O43511, (Rat) Q9R154, (Mouse) Q9R155
Entrez Gene ID: (Human) 5172, (Rat) 29440, (Mouse) 23985
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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