C1orf129 Rabbit pAb, Biotin conjugated(bs-9778R-Bio)-100ul

C1orf129 Rabbit pAb, Biotin co

njugated(bs-9778R-Bio)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-9778R-Bio
  • 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-9778R-Bio
    英文名称C1orf129 Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的1号染色体开放阅读框129抗体
    英文别名Armadillo repeat containing 11; ARMC11; CA129_HUMAN; Chromosome 1 open reading frame 129; FLJ23550; RP5-1092L12.1; Uncharacterized protein C1orf129; ARMC11; MROH9; maestro heat like repeat family member 9.
    产品应用WB=1:500-2000

    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 C1orf129
    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.
    相似性Contains 5 HEAT repeats.
    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Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf129 gene product has been provisionally designated C1orf129 pending further characterization.

     

    应用推荐稀释比例
    {WB}{1:500-2000}

     

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