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Antibody detects endogenous levels of total CLCNKB.
Chloride channel Kb (CLCNKB) is a member of the CLC family of voltage-gated chloride channels, which comprises at least 9 mammalian chloride channels. Each is believed to have 12 transmembrane domains and intracellular N and C termini. Mutations in CLCNKB result in the autosomal recessive Type III Bartter Syndrome. CLCNKA and CLCNKB are closely related (94% sequence identity), tightly linked (separated by 11 kb of genomic sequence) and are both expressed in mammalian kidney.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Chloride channel Kb; Chloride channel protein ClC-Kb; chloride channel, kidney, B; chloride channel, voltage-sensitive Kb; ClC-K2; CLCNK; hClC-Kb; MGC24087; RP11-5P18.8
Gene Aliases: ClC-K2; ClC-Kb; CLCKB; CLCNKB
UniProt ID: (Human) P51801
Entrez Gene ID: (Human) 1188
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