BSND 蛋白
(Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))
This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness. [provided by RefSeq, Jul 2008].
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custom-made
BSND
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, ELISA, WB
custom-made
BSND
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, ELISA, WB
Aliases for BSND 蛋白
Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND) 蛋白barttin CLCNK type accessory beta subunit (BSND) 蛋白
barttin CLCNK type accessory beta subunit (Bsnd) 蛋白
BART 蛋白
BSND 蛋白
DFNB73 蛋白
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