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DFNB31 抗体 (Center)

DFNB31 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2797202
发货至: 中国
  • 抗原 See all DFNB31 抗体
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    抗原表位
    • 7
    • 7
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 378-406, Center
    适用
    • 28
    • 3
    宿主
    • 26
    • 4
    克隆类型
    • 27
    • 3
    多克隆
    标记
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNB31 antibody is un-conjugated
    应用范围
    • 23
    • 18
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    原理
    Rabbit Anti-Human DFNB31 (Center) Antibody
    免疫原
    This DFNB31 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 378-406 amino acids from the Central region of human DFNB31.
    亚型
    Ig Fraction
    Top Product
    Discover our top product DFNB31 Primary Antibody
  • 应用备注
    Western Blot, Immunohistochemistry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50Western blot analysis of lysate from human kidney tissue lysate, using DFNB31 Antibody (Center) for immunohistochemistry. Clinical relevance has not been evaluated.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5 mg/mL
    储存条件
    4 °C,-20 °C
    储存方法
    2-8°C (short-term), -20°C (long-term)
  • 抗原
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    别名
    DFNB31 (DFNB31 产品)
    别名
    DFNB31 antibody, CIP98 antibody, PDZD7B antibody, USH2D antibody, WHRN antibody, WI antibody, Cip98 antibody, Whrn antibody, 1110035G07Rik antibody, AW122018 antibody, AW742671 antibody, C430046P22Rik antibody, Dfnb31 antibody, wi antibody, whirlin antibody, WHRN antibody, LOC100555508 antibody, Whrn antibody
    背景

    Target Description: 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.

    Gene Symbol: DFNB31

    分子量
    96586 Da
    基因ID
    25861
    UniProt
    Q9P202
    途径
    Sensory Perception of Sound
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