HAP1 Rabbit pAb, APC-Cy5.5 conjugated(bs-20303R-APC-Cy5.5)-100ul

HAP1 Rabbit pAb, APC-Cy5.5 con

jugated(bs-20303R-APC-Cy5.5)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-20303R-APC-Cy5.5
  • 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-20303R-APC-Cy5.5
    英文名称HAP1 Rabbit pAb, APC-Cy5.5 conjugated
    中文名称APC-Cy5.5标记的舞蹈症相关蛋白1抗体
    英文别名Huntingtin Associated Protein 1; HAP 1; HAP 2; HAP2; HAP-1; Hap1; HAP1_HUMAN; HAPP; hHAP1; hHLP1; HIP 5; HIP5; HLP; HLP1; Huntingtin-associated protein 1; huntingtin-associated protein 2; Neuroan 1; Neuroan1.
    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 HAP1
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
    研究领域

    Neuroscience > Neurology process > Neurodegenerative disease > Huntington's disease

    Neuroscience > Neurology process > Neurogenesis

    Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation

    组织特异性Predominantly expressed in brain. Selectively expressed in neurons.
    相似性Contains 1 HAP1 N-terminal domain.
    功能Associates specifically with huntingtin. This binding is enhanced by an expanded polyglutamine repeat.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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