SOX10 Recombinant Rabbit mAb, IRDye 800CW conjugated(bsm-52229R-IRDye800CW)-100ul

SOX10 Recombinant Rabbit mAb,

IRDye 800CW conjugated(bsm-52229R-IRDye800CW)-100ul
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  • ¥3200
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  • bsm-52229R-IRDye800CW
  • 2025年12月01日
  • 产品信息以Bioss网站为准
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    • 规格

      100ul

    产品编号bsm-52229R-IRDye800CW
    英文名称SOX10 Recombinant Rabbit mAb, IRDye 800CW conjugated
    中文名称IRDye 800CW标记的转录因子SOX10重组兔单抗
    英文别名DOM; MGC15649; SOX 10; SOX10_HUMAN; SRY(sex determining region Y) box 10; SRY box containing gene 10; SRY related HMG box gene 10; Transcription factor SOX 10; Transcription factor SOX-10; WS4.
    产品应用WB=1:1000-5000

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

    抗体来源Rabbit
    免疫原A synthesized peptide derived from human SOX10
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Recombinant
    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 > Lineage specification > Ectoderm

    Epigenetics and Nuclear Signaling > Transcription > Domain Families > HMG Box

    Neuroscience > Cell Type Marker > Neural Stem Cell marker

    Stem Cells > Lineage Markers > Ectoderm

    亚细胞定位Cytoplasm. Nucleus
    组织特异性Expressed in fetal brain and in adult brain, heart, small intestine and colon.
    相似性Contains 1 HMG box DNA-binding domain.
    功能Transcription factor that seems to function synergistically with the POU domain protein TST-1/OCT6/SCIP. Could confer cell specificity to the function of other transcription factors in developing and mature glia.
    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 member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]

     

    应用推荐稀释比例
    {WB}{1:1000-5000}

     

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