TSPAN9 Rabbit pAb(bs-9448R)-50ul/100ul/200ul

TSPAN9 Rabbit pAb(bs-9448R)-50

ul/100ul/200ul
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  • ¥1180 - 2800
  • Bioss已认证
  • bs-9448R
  • 2025年10月24日
  • 产品信息以Bioss网站为准
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    • 规格

      50ul/100ul/200ul

    规格:50ul产品价格:¥1180.0
    规格:100ul产品价格:¥1980.0
    规格:200ul产品价格:¥2800.0
    产品编号bs-9448R
    英文名称TSPAN9 Rabbit pAb
    中文名称四分子交联体9/四旋蛋白抗体
    英文别名Tetraspanin 9; NET 5; NET5; PP1057; Tetraspan NET 5; Tetraspan NET-5; Tetraspanin-9; Transmembrane 4 superfamily member tetraspan NET 5; TSN9_HUMAN; Tspan-9; TSPAN9.
    产品应用ELISA=1:5000-10000

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

    交叉反应Human (Mouse, Rat, Dog, Pig, Rabbit)
    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human TSPAN9
    亚型IgG
    性状Liquid
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    理论分子量27 kDa
    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

    Signal Transduction > Adapters > Transmembrane

    亚基Found in a complex with GP6.
    亚细胞定位Membrane; Multi-pass membrane protein.
    组织特异性Expressed in megakaryocytes and platelets.
    相似性Belongs to the tetraspanin (TM4SF) family.
    保存条件Shipped at 4℃. Store at -20℃ 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The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

     

    应用推荐稀释比例
    {ELISA}{1:5000-10000}

     

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    TSPAN9 Rabbit pAb(bs-9448R)-50ul/100ul/200ul
    ¥1180 - 2800