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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Pendrin; Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4
基因别名: PDS; SLC26A4
Entrez Gene ID: (Human) 5172