概述

  • 产品名称Anti-CAMSAP1抗体
    参阅全部 CAMSAP1 一抗
  • 描述
    兔多克隆抗体to CAMSAP1
  • 经测试应用适用于: WB, IPmore details
  • 种属反应性
    与反应: Human
    预测可用于: Rhesus monkey, Gorilla, Orangutan
  • 免疫原

    A synthetic papetide corresponding to a region between residues 1050 and 1100 of Human CAMSAP1 using the numbering given in entry NP_056262.3

  • 阳性对照
    • HeLa whole cell lysate

性能

  • 形式Liquid
  • 存放说明Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
  • 存储溶液Preservative: 0.09% Sodium Azide
    Constituents: 0.1% BSA, Tris buffered saline
  • Concentration information loading...
  • 纯度Immunogen affinity purified
  • 克隆多克隆
  • 同种型IgG
  • 研究领域

相关产品

应用

Our Abpromise guarantee covers the use of ab86000 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 1/2000 - 1/10000. Predicted molecular weight: 117 kDa.
IP Use at 3-5 µg/mg of lysate.

靶标

  • 序列相似性Belongs to the CAMSAP1 family.
    Contains 1 CH (calponin-homology) domain.
    Contains 1 CKK domain.
  • 结构域The CKK domain binds microtubules.
  • 细胞定位Cytoplasm > cytoskeleton.
  • Information by UniProt
  • 数据库链接
  • 别名
    • calmodulin regulated spectrin-associated protein 1 antibody
    • Calmodulin-regulated spectrin-associated protein 1 antibody
    • CAMP1_HUMAN antibody
    • camsap1 antibody
    • PRO2405 antibody
    see all

Anti-CAMSAP1 antibody 图像

  • All lanes : Anti-CAMSAP1 antibody (ab86000) at 0.04 µg/ml

    Lane 1 : HeLa whole cell lysate at 50 µg
    Lane 2 : HeLa whole cell lysate at 15 µg
    Lane 3 : HeLa whole cell lysate at 5 µg


    Predicted band size : 117 kDa
  • Detection of Human CAMSAP1 by immunoprecipitation, using ab86000 at 3µg/ml HeLa whole cell lysate, 1 mg lysate used for immunoprecipitation, 20% loaded (Lane 1). Control IgG (Lane 2). Detection by chemiluminescence with exposure time of 30 seconds.

Anti-CAMSAP1 antibody (ab86000)参考文献

ab86000 has not yet been referenced specifically in any publications.

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