产品中心 流式试剂&相关 流式抗体

所有图片(1/1)

Alexa Fluor® 647 Rat Anti-Mouse CD106 Antibody (S-R733)

Vascular cell adhesion protein 1,V-CAM 1,VCAM-1Cleaved into 1 chainsSoluble Vascular Cell Adhesion Molecule-1,Vcam-1,Vcam1

价格 780.00 供应商现货 : 3-5个工作日
货号 S0B80379
规格
数量
收藏 分享

产品介绍 评论(0)

产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD106
  • 分子别名

    Vascular cell adhesion protein 1; V-CAM 1; VCAM-1Cleaved into 1 chainsSoluble Vascular Cell Adhesion Molecule-1; Vcam-1; Vcam1
  • 细胞定位

    Secreted, Cell membrane
  • Accession

    P29533
  • 克隆号

    S-R733
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 同型对照

    S0B8044
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse bone marrow
  • 纯化方式

    Protein G
  • 浓度

    0.5 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 1μg per million cells in 100μl volume Ms
背景介绍
  • CD106, also known as vascular cell adhesion molecule-1 (VCAM-1), is a member of the immunoglobulin superfamily of proteins and is predominantly expressed in endothelial cells. It is a cytokine-inducible cell surface protein capable of mediating adhesion to leukocytes expressing alpha 4 integrins. CD106 plays a crucial role in various physiological and pathological processes. In embryonic development, CD106-deficient mouse embryos are not viable, showing severe defects in placental and heart development. In immune regulation, CD106 is involved in T cell activation and leukocyte recruitment to inflammation sites. It is also critical for mesenchymal stem cells (MSCs)-mediated immunosuppression and the binding of hematopoietic progenitor cells.

  • 流式分析

    • Flow cytometric analysis of mouse CD106 expression on C57BL/6 mouse bone marrow. C57BL/6 mouse bone marrow were stained with Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse CD106 Antibody (right panel) at 2 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

评论(0)