WRB Rabbit pAb, Cy7 conjugated(bs-11774R-Cy7)-100ul

WRB Rabbit pAb, Cy7 conjugated

(bs-11774R-Cy7)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-11774R-Cy7
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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    • 规格

      100ul

    产品编号bs-11774R-Cy7
    英文名称WRB Rabbit pAb, Cy7 conjugated
    中文名称Cy7标记的色氨酸丰富蛋白抗体
    英文别名Chromodomain helicase DNA binding protein 5; CHD5; Congenital heart disease 5 gene; Congenital heart disease 5 protein; FLJ51808; Tryptophan rich basic protein; Tryptophan rich protein, congenital heart disease 5 protein; WRB; WRB_HUMAN.
    产品应用Flow-Cyt=2ug/Test, 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 WRB/Tryptophan rich protein
    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.
    亚基Interacts with ASNA1/TRC40.
    亚细胞定位Nucleus. Membrane; Multi-pass membrane protein
    相似性Belongs to the WRB/GET1 family.
    功能This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrom congenital heart disease.
    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 basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009].

     

    应用推荐稀释比例
    {Flow-Cyt}{2ug/Test}
    {IF}{1:100-500}

     

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