CEP120 Rabbit pAb, BF488 conjugated(bs-13850R-BF488)-100ul

CEP120 Rabbit pAb, BF488 conju

gated(bs-13850R-BF488)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-13850R-BF488
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-13850R-BF488
    英文名称CEP120 Rabbit pAb, BF488 conjugated
    中文名称BF488标记的中心体蛋白CEP120抗体
    英文别名CCDC100; CE120_HUMAN; Centrosomal protein of 120 kDa; Cep120; Coiled-coil domain-containing protein 100.
    产品应用IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human CEP120
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Developmental Biology > Organogenesis > Nervous system development

    Signal Transduction > Protein Trafficking > Organelle Proteins

    Tags & Cell Markers > Subcellular Markers > Organelles > Centrosome

    亚细胞定位Cytoplasm > cytoskeleton > centrosome. Regulates the localization of TACC3 to the centrosome in neural progenitors in vivo.
    相似性Belongs to the CEP120 family.
    功能Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. May play a role in centriole duplication during mitosis.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料This gene encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. A similar protein in mouse plays a role in both interkinetic nuclear migration, which is a characteristic pattern of nuclear movement in neural progenitors, and in neural progenitor self-renewal. Mutations in this gene are predicted to result in neurogenic defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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