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DFNB31 ELISA试剂盒

(Deafness, Autosomal Recessive 31 (DFNB31))
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].

3 results

DFNB31 适用: 人 Colorimetric
产品编号 ABIN1167470
 
DFNB31 适用: 大鼠 Colorimetric
产品编号 ABIN1167472
 
DFNB31 适用: 小鼠 Colorimetric
产品编号 ABIN1167471
 
  • 类型 Kit
    • Kit
  • 应用范围 ELISA
    • ELISA
  • 适用
    • Human
    • Mouse
    • Rat
  • 检测方法
    • Colorimetric
  • Plate
    • Pre-coated
  • 标记
    • 非结合性
  • Supplier
    • EIAab

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