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This antibody detects endogenous protein at a molecular weight of 75 kDa.
Purity is >95% by SDS-PAGE.
CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter's syndrome which is characterized by renal salt-wasting and low blood pressure.
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: chloride channel K1; Chloride channel Ka; Chloride channel protein ClC-Ka; chloride channel, kidney, A; chloride channel, voltage-sensitive Ka; ClC-K1; CLC-KA; CLCKA
基因别名: ClC-K1; CLCK1; Clcnk1; CLCNKA; hClC-Ka
UniProt ID: (Human) P51800, (Rat) Q06393
Entrez Gene ID: (Human) 1187, (Rat) 79425