FAM70A Rabbit pAb, Cy3 conjugated(bs-11006R-Cy3)-100ul

FAM70A Rabbit pAb, Cy3 conjuga

ted(bs-11006R-Cy3)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-11006R-Cy3
  • 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-11006R-Cy3
    英文名称FAM70A Rabbit pAb, Cy3 conjugated
    中文名称Cy3标记的FAM70A蛋白抗体
    英文别名family with sequence similarity 70, member A; FLJ20716; hypothetical protein T255A_HUMAN.
    产品应用ICC/IF=1:50-200, 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 FAM70A
    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.
    亚细胞定位Membrane; Multi-pass membrane protein
    相似性Belongs to the TMEM255 family.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM70A gene product has been provisionally designated FAM70A pending further characterization.

     

    应用推荐稀释比例
    {ICC/IF}{1:50-200}
    {IF}{1:100-500}

     

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