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Centrosomal Protein 57kDa (CEP57) (Middle Region) Peptide

CEP57 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5511672
发货至: 中国
  • 抗原 See all CEP57 products
    CEP57 (Centrosomal Protein 57kDa (CEP57))
    蛋白结构域
    Middle Region
    宿主
    资源
    • 2
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    RLIFEDKATP CVPNARRIKK KKSKPPEKKS SRNYFGAQPH YRLCLGDMPF
    产品特性
    This is a synthetic peptide designed for use in combination with anti-CEP57 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    CEP57 (Centrosomal Protein 57kDa (CEP57))
    别名
    3110002L15RIK Peptide, CEP57 Peptide, cep57r Peptide, xCep57 Peptide, c6orf182 Peptide, 3110002l15rik Peptide, RGD1309884 Peptide, 3110002L15Rik Peptide, 4921510P06Rik Peptide, 4931428M20Rik Peptide, AI467480 Peptide, Tsp57 Peptide, mKIAA0092 Peptide, MVA2 Peptide, PIG8 Peptide, TSP57 Peptide, centrosomal protein 57 Peptide, centrosomal protein 57kDa-like 1 Peptide, CEP57 Peptide, cep57l1 Peptide, Cep57 Peptide
    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.

    Alias Symbols: CEP57,KIAA0092, TSP57,

    Protein Size: 500
    基因ID
    9702
    NCBI登录号
    NP_055494
    UniProt
    Q86XR8
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