BSND 产品
(Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))
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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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Featured BSND Categories
BSND 抗体
High quality antibodies with extensive validation data.
BSND ELISA试剂盒
Reliable ELISA kits for a wide range of species.
BSND 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended BSND 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC (p)
Validations
- (3)
Cat. No.
ABIN521643
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (3)
Cat. No.
ABIN6137670
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human, Mouse
Application
WB, IHC (p)
Validations
- (4)
Cat. No.
ABIN653815
Quantity
400 μL
Datasheet
Datasheet
Recommended BSND ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Validations
Cat. No.
ABIN1123296
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Mouse
Analytical Method
Validations
Cat. No.
ABIN1123297
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Rat
Analytical Method
Validations
Cat. No.
ABIN1123298
Quantity
96 tests
Datasheet
Datasheet
Recommended BSND 蛋白
Synonyms and alternative names related to BSND
Bartter syndrome, infantile, with sensorineural deafness (Barttin) (BSND), barttin CLCNK type accessory beta subunit (BSND), barttin CLCNK type accessory beta subunit (Bsnd), BART, BSND, DFNB73Protein level used designations for BSND
- Bartter syndrome, infantile, with sensorineural deafness (Barttin)
- barttin
- deafness, autosomal recessive 73
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