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Otoraplin 抗体 (AA 11-100)

OTOR 适用: 人 ELISA, IHC (p), IF (cc), IF (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN721870
发货至: 中国
  • 抗原 See all Otoraplin (OTOR) 抗体
    Otoraplin (OTOR)
    抗原表位
    AA 11-100
    适用
    • 9
    • 3
    宿主
    • 10
    克隆类型
    • 10
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Otoraplin antibody is un-conjugated
    应用范围
    ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human Otoraplin/Fibrocyte derived protein
    亚型
    IgG
    Top Product
    Discover our top product OTOR Primary Antibody
  • 应用备注
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    Otoraplin (OTOR)
    别名
    Otoraplin (OTOR 产品)
    别名
    FDP antibody, MIAL1 antibody, CDRAP antibody, Fdp antibody, MIA antibody, MIAL antibody, MGC133655 antibody, MGC86203 antibody, otoraplin antibody, otoraplin L homeolog antibody, OTOR antibody, Otor antibody, otor.L antibody, otor antibody
    背景

    Synonyms: Fibrocyte derived protein,Melanoma inhibitory activity like protein,FDP,Fibrocyte-derived protein,Melanoma inhibitory activity-like protein,MIAL,OTOR,OTOR_HUMAN,Otoraplin.

    Background: The protein encoded by this gene is secreted via the Golgi apparatus and may function in cartilage development and maintenance. A frequent polymorphism in the translation start codon of this gene can abolish translation and may be associated with forms of deafness. This gene is a member of the melanoma-inhibiting activity gene family. In addition, alternate polyA sites exist for this gene. [provided by RefSeq, Jul 2008].

    基因ID
    56914
    途径
    Sensory Perception of Sound, Regulation of Carbohydrate Metabolic Process
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