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DFNB31 抗体 (AA 378-406)

DFNB31 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB19059 unconjugated
产品编号 ABIN655065
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
    • 1
    AA 378-406
    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
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    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.
    克隆位点
    RB19059
    亚型
    Ig Fraction
    Top Product
    Discover our top product DFNB31 Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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.
    储存条件
    4 °C,-20 °C
    储存方法
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    有效期
    6 months
  • 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
    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.
    分子量
    96558
    基因ID
    25861
    NCBI登录号
    NP_001077354, NP_001166896, NP_056219
    UniProt
    Q9P202
    途径
    Sensory Perception of Sound
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