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Alexa Fluor® 647 Mouse Anti-Human CD106 Antibody (S-2895)

Vascular cell adhesion protein 1,V-CAM 1,VCAM-1,INCAM-100,VCAM1

价格 500.00 供应商现货 : 3-5个工作日
货号 S0B5599
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD106
  • 分子别名

    Vascular cell adhesion protein 1; V-CAM 1; VCAM-1; INCAM-100; VCAM1
  • 细胞定位

    Cell membrane, Secreted
  • Accession

    P19320
  • 克隆号

    S-2895
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 阳性样本

    HUVEC treated with TNF-α
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1.25μl per million cells in 100μl volume Hu
背景介绍
  • CD106, also known as vascular cell adhesion molecule 1 (VCAM-1), is a protein encoded by the VCAM1 gene in humans and belongs to the immunoglobulin superfamily. It is a cytokine-inducible cell surface protein that mediates the adhesion of leukocytes to vascular endothelium, playing a crucial role in immune responses and inflammation. CD106 is primarily expressed on endothelial cells, but its expression can also be found in other cell types such as smooth muscle cells and mesenchymal stem cells. The upregulation of CD106 in endothelial cells is induced by cytokines like tumor necrosis factor-alpha (TNF-α) and interleukin-1 (IL-1), and it is involved in various pathological conditions, including atherosclerosis and rheumatoid arthritis. In addition, CD106 is essential for embryonic development, particularly in the formation of the umbilical cord and placenta.

  • 流式分析

    • Flow cytometric analysis of CD106 expression on HUVEC cells. HUVEC were either untreated (Left Panel) or treated 20 hours with 10 ng/ml Human TNF-α protein (Right Panel) and then stained with Mouse IgG1, κ Isotype Control (Black line histogram) or SDT Alexa Fluor® 647 Mouse Anti-Human CD106 Antibody at 1.25 μl/test (Red line histogram). Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software

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