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NeuN Rabbit pAb, PE conjugated

(bs-1613R-PE)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-1613R-PE
  • 2025年10月15日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-1613R-PE
    英文名称NeuN Rabbit pAb, PE conjugated
    中文名称PE标记的神经元核抗原抗体
    英文别名RFOX3_HUMAN; RNA binding protein fox-1 homolog 3; RBFOX3; Fox-1 homolog C; Neuronal nuclei antigen(NeuN antigen); FOX3; FOX-3; HRNBP3;
    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 NeuN
    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

    Epigenetics and Nuclear Signaling > Transcription > Domain Families > Forkhead Box > Other FOXes

    Epigenetics and Nuclear Signaling > Transcription > Transcription Factors

    Neuroscience > Cell Type Marker > Neuron marker > Soma marker

    Signal Transduction > Antibodies > neun

    Tags & Cell Markers > Cell Type Markers > Neuroscience Markers > Neuronal

    亚细胞定位Nucleus. Cytoplasm.
    组织特异性Expressed in activated, but not resting, CD4+ T-cells and activated monocytes.
    相似性Contains 1 RRM (RNA recognition motif) domain.
    功能RNA-binding protein that regulates alternative splicing events.
    保存条件Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料This gene encodes a member of the RNA-binding FOX protein family which is involved in the regulation of alternative splicing of pre-mRNA. The protein has an N-terminal proline-rich region, an RNA recognition motif (RRM) domain, and a C-terminal alanine-rich region. This gene produces the neuronal nuclei (NeuN) antigen that has been widely used as a marker for post-mitotic neurons. This gene has its highest expression in the central nervous system and plays a prominent role in neural tissue development and regulation of adult brain function. Mutations in this gene have been associated with numerous neurological disorders. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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