概述

  • 产品名称Anti-MS4A14抗体
    参阅全部 MS4A14 一抗
  • 描述
    兔多克隆抗体to MS4A14
  • 经测试应用适用于: WBmore details
  • 种属反应性
    与反应: Human
  • 免疫原

    Synthetic peptide corresponding to a region within internal sequence amino acids 576 - 625 (

    YPEGQSKDGQVKDQQTDKEQNSKKQTQDQQTEDQPAQEKKSPKGQFQNVQ

    ) of Human MS4A14 (NP_115986)

  • 阳性对照
    • PANC1 cell lysate

性能

  • 形式Liquid
  • 存放说明Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
  • 存储溶液Preservative: None
    Constituents: 2% Sucrose, PBS
  • Concentration information loading...
  • 纯度Immunogen affinity purified
  • 克隆多克隆
  • 同种型IgG
  • 研究领域

应用

Our Abpromise guarantee covers the use of ab90010 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
WB Use a concentration of 1 µg/ml. Predicted molecular weight: 77 kDa. Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T.

靶标

  • 相关性MS4A14 may be involved in signal transduction as a component of a multimeric receptor complex.
  • 细胞定位Membrane; Multi-pass membrane protein
  • 数据库链接
  • 别名
    • FLJ32856 antibody
    • Membrane spanning 4 domains subfamily A member 14 antibody
    • Membrane spanning 4 domains subfamily A member 16 antibody
    • MGC104289 antibody
    • MGC49828 antibody
    • MS4A13 antibody
    • MS4A13 protein antibody
    • MS4A16 antibody
    • NYD SP21 antibody
    • NYDSP21 antibody
    • Testis development protein NYD SP21 antibody
    • Testis development protein NYDSP21 antibody
    • Testis development related NYD SP21 antibody
    • Testis development related NYDSP21 antibody
    see all

Anti-MS4A14 antibody 图像

  • Anti-MS4A14 antibody (ab90010) at 1 µg/ml (in 5% skim milk / PBS buffer) + PANC1 cell lysate at 10 µg

    Secondary
    HRP conjugated anti-Rabbit IgG at 1/50000 dilution

    Predicted band size : 77 kDa

Anti-MS4A14 antibody (ab90010)参考文献

ab90010 has not yet been referenced specifically in any publications.

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