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FOXI1 抗体

FOXI1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7248701
发货至: 中国
  • 抗原 See all FOXI1 抗体
    FOXI1 (Forkhead Box I1 (FOXI1))
    适用
    • 62
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    宿主
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    克隆类型
    • 59
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    多克隆
    标记
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    This FOXI1 antibody is un-conjugated
    应用范围
    • 33
    • 25
    • 13
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    • 5
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    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human FOXI1
    亚型
    IgG
    Top Product
    Discover our top product FOXI1 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.62 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    FOXI1 (Forkhead Box I1 (FOXI1))
    别名
    FOXI1 (FOXI1 产品)
    别名
    FKH10 antibody, FKHL10 antibody, FREAC-6 antibody, FREAC6 antibody, HFH-3 antibody, HFH3 antibody, 5830401E05Rik antibody, Fkh10 antibody, Hfh3 antibody, cb724 antibody, foo antibody, Xfoxi1a antibody, ema antibody, foxi1a antibody, foxi1e antibody, xema antibody, xfoxi1 antibody, FoxI1e antibody, Xema antibody, fkhl10 antibody, freac6 antibody, hfh3 antibody, FOXI1 antibody, forkhead box I1 antibody, forkhead box i1 antibody, forkhead box I1 L homeolog antibody, forkhead box protein I1 antibody, FOXI1 antibody, Foxi1 antibody, foxi1 antibody, foxi1.L antibody, CC1G_14832 antibody
    背景
    This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 41 kDa

    UniProt
    Q12951
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