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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.
Immunogen sequence: FGLLTVVLRV QFPSWNGLGS IPSTDIYKST KNYKNIEEPQ GVKILRFSSP IFYGNVDGFK KCIKSTVGFD AIRVYNKRLK ALRK
Highest antigen sequence identity to the following orthologs: Mouse - 89%, Rat - 90%.
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: Pendrin; Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4
Gene Aliases: PDS; SLC26A4
Entrez Gene ID: (Human) 5172
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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