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EVC2 抗体 (C-Term)

This anti-EVC2 antibody (ABIN2856532) is a Rabbit Polyclonal antibody detecting EVC2 in WB, IF, ICC. Suitable for Human.
产品编号 ABIN2856532
发货至: 中国

Quick Overview for EVC2 抗体 (C-Term) (ABIN2856532)

抗原

See all EVC2 抗体
EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))

适用

宿主

  • 13
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克隆类型

  • 14
多克隆

标记

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This EVC2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)
  • 抗原表位

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    C-Term

    交叉反应

    小鼠

    交叉反应 (详细)

    Mouse (85 %)

    产品特性

    Rabbit Polyclonal antibody to EVC2 (Ellis van Creveld syndrome 2)
    EVC2 antibody [C3], C-term

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human EVC2. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    Suggested dilution Reference ICC/IF 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* Western blot1:500-1:3000*

    说明

    Positive Control: A431 , H1299 , HeLa , HepG2

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))

    别名

    EVC2

    背景

    This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.

    Cellular Localization: Membrane, Multi-pass membrane protein

    分子量

    148 kDa

    基因ID

    132884

    途径

    Hedgehog Signaling
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