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DFNB31 抗体 (Middle Region)

DFNB31 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN955575
发货至: 中国
  • 抗原 See all DFNB31 抗体
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    抗原表位
    • 7
    • 7
    • 6
    • 6
    • 3
    • 1
    • 1
    • 1
    AA 385-413, Middle Region
    适用
    • 27
    • 3
    宿主
    • 25
    • 4
    克隆类型
    • 26
    • 3
    多克隆
    标记
    • 12
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNB31 antibody is un-conjugated
    应用范围
    • 22
    • 18
    • 14
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
    特异性
    This antibody recognizes Human Whirlin (Center).
    纯化方法
    Affinity Chromatography on Protein A
    免疫原
    KLH conjugated synthetic peptide between 385-413 amino acids from the Central region of Human Whirlin. Genename: WHRN
    亚型
    Ig Fraction
    Top Product
    Discover our top product DFNB31 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.25 mg/mL
    缓冲液
    PBS, 0.09 % Sodium Azide
    储存液
    Sodium azide
    注意事项
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原
    DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
    别名
    Whirlin (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
    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.Synonyms: Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
    分子量
    96586 Da
    基因ID
    25861
    NCBI登录号
    NP_001077354
    途径
    Sensory Perception of Sound
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