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CEP57 抗体

This anti-CEP57 antibody is a 兔 多克隆 antibody detecting CEP57 in WB 和 ELISA. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7246166
发货至: 中国

Quick Overview for CEP57 抗体 (ABIN7246166)

抗原

See all CEP57 抗体
CEP57 (Centrosomal Protein 57kDa (CEP57))

适用

  • 45
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 41
  • 4

克隆类型

  • 44
  • 1
多克隆

标记

  • 20
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CEP57 antibody is un-conjugated

应用范围

  • 23
  • 19
  • 13
  • 13
  • 6
  • 5
  • 5
  • 3
  • 3
  • 2
Western Blotting (WB), ELISA
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Full length fusion protein

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.42 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    CEP57 (Centrosomal Protein 57kDa (CEP57))

    别名

    CEP57

    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 alternatively spliced transcript variants encoding different isoforms have been identified.

    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 57 kDa

    UniProt

    Q86XR8

    途径

    M Phase, Maintenance of Protein Location, Protein targeting to Nucleus, Growth Factor Binding
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