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C7orf42 抗体 (AA 231-314)

This 兔 多克隆 anti-C7orf42 antibody specifically detects C7orf42 in WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p) 和 ICC. The antibody is reactive with 人 samples.
产品编号 ABIN1714128
发货至: 中国
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Quick Overview for C7orf42 抗体 (AA 231-314) (ABIN1714128)

抗原

C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

适用

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宿主

  • 24

克隆类型

  • 24
多克隆

标记

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This C7orf42 antibody is un-conjugated

应用范围

Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
  • 抗原表位

    • 14
    • 3
    AA 231-314

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C7orf42

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    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
    ICC 1:100-500

    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

    C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

    别名

    C7orf42

    背景

    Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.

    Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.

    基因ID

    55069
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