DFNB31 产品
(Deafness, Autosomal Recessive 31 (DFNB31))
Categories
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Mar 2010].
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Featured DFNB31 Categories
DFNB31 抗体
High quality antibodies with extensive validation data.
DFNB31 ELISA试剂盒
Reliable ELISA kits for a wide range of species.
Recommended DFNB31 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (2)
Cat. No.
ABIN565193
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA, IF
Validations
- (2)
Cat. No.
ABIN525468
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (1)
Cat. No.
ABIN525467
Quantity
50 μL
Datasheet
Datasheet
Recommended DFNB31 ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Validations
Cat. No.
ABIN1167470
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Mouse
Analytical Method
Validations
Cat. No.
ABIN1167471
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Rat
Analytical Method
Validations
Cat. No.
ABIN1167472
Quantity
96 tests
Datasheet
Datasheet
Recommended DFNB31 蛋白
Synonyms and alternative names related to DFNB31
whirlin (WHRN), whirlin (LOC100555508), whirlin (Whrn), 1110035G07Rik, AW122018, AW742671, C430046P22Rik, CIP98, Cip98, DFNB31, Dfnb31, PDZD7B, USH2D, WHRN, Whrn, WI, wiProtein level used designations for DFNB31
- deafness, autosomal recessive 31
- CASK-interacting protein CIP98
- whirlin-like
- autosomal recessive deafness type 31 protein
- whirlin
- whirler
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