Background：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 results in multiple transcript variants.
仕様
Synonyms：Whirlin,Autosomal Recessive Deafness Type 31 Protein,DFNB31,Deafness Autosomal Recessive 31,CASK-Interacting Protein CIP98,KIAA1526,PDZD7B,CIP98,USH2D,WI,WHRN,KIAA1526
Host：Rabbit
Reactivity：Human,Mouse
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human WHRN
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
