FoxC1/2 Polyclonal Antibody

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¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2614088

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商品描述
  • 靶点-Target

    FoxC1/2

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,IHC,IF,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    57kD

  • 推荐稀释比

    WB 1:500-1:2000;IHC 1:100-1:300;IF 1:200-1:1000;ELISA 1:40000;Not yet tested in other applications.

  • 组成

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • 纯化工艺

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 浓度

    1 mg/ml

  • 克隆性

    Polyclonal

  • 免疫原

    The antiserum was produced against synthesized peptide derived from human FOXC1/2. AA range:151-200

  • 特异性

    FoxC1/2 Polyclonal Antibody detects endogenous levels of FoxC1/2 protein.

  • 基因名称

    FOXC1/FOXC2

  • 蛋白名称

    Forkhead box protein C1/2

  • 别名

    FOXC1;FKHL7;FREAC3;Forkhead box protein C1;Forkhead-related protein FKHL7;Forkhead-related transcription factor 3;FREAC-3;FOXC2;FKHL14;MFH1;Forkhead box protein C2;Forkhead-related protein FKHL14;Mesenchyme fork head protein 1;

  • Organism-1

    Human

  • 基因ID-1

    2296;2303

  • SwissProt-1

    Q12948;Q99958

  • Organism-2

    Mouse

  • 基因ID-2

    17300;14234

  • Organism-3

    Rat

  • SwissProt-3

    Q63246

  • 背景

    This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly. [provided by RefSeq, Jul 2008],

  • 细胞定位

    Nucleus . Colocalizes with PITX2 isoform 3 in the nucleus at subnuclear chromatine regions (PubMed:16449236). Colocalizes with CBX5 to a heterochromatin-rich region of the nucleus (PubMed:15684392). Colocalizes with GLI2 in the nucleus (By similarity). .