CEP57 Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2613342

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商品描述
  • 靶点-Target

    CEP57

  • 反应性

    Human,Rat,Mouse,

  • 应用

    WB,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    50kD

  • 推荐稀释比

    WB 1:500-1:2000;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 CEP57. AA range:241-290

  • 特异性

    CEP57 Polyclonal Antibody detects endogenous levels of CEP57 protein.

  • 基因名称

    CEP57

  • 蛋白名称

    Centrosomal protein of 57 kDa

  • 别名

    CEP57;KIAA0092;TSP57;Centrosomal protein of 57 kDa;Cep57;FGF2-interacting protein;Testis-specific protein 57;Translokin

  • Organism-1

    Human

  • 基因ID-1

    9702

  • SwissProt-1

    Q86XR8

  • Organism-2

    Mouse

  • SwissProt-2

    Q8CEE0

  • 背景

    This gene encodes a cytoplasmic protein called Translokin. This protein localizes to the centrosome and has a function in microtubular stabilization. The N-terminal half of this protein is required for its centrosome localization and for its multimerization, and the C-terminal half is required for nucleating, bundling and anchoring microtubules to the centrosomes. This protein specifically interacts with fibroblast growth factor 2 (FGF2), sorting nexin 6, Ran-binding protein M and the kinesins KIF3A and KIF3B, and thus mediates the nuclear translocation and mitogenic activity of the FGF2. It also interacts with cyclin D1 and controls nucleocytoplasmic distribution of the cyclin D1 in quiescent cells. This protein is crucial for maintaining correct chromosomal number during cell division. Mutations in this gene cause mosaic variegated aneuploidy syndrome, a rare autosomal recessive disorder. Multiple

  • 细胞定位

    Nucleus . Cytoplasm. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome .