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PE-Cy7 Rat Anti-Mouse Ly-6C Antibody (S-R523)

PE-Cy7 Rat Anti-Mouse Ly-6C Antibody (S-R523)

货号: S0B1814
价格: 1060
规格: 25T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    Mouse Ly-6C
  • 分子别名

    Lymphocyte antigen 6C1; Ly-6C1
  • 细胞定位

    Cell membrane
  • Accession

    P0CW02
  • 克隆号

    S-R523
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2c,k
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    PE-Cy7
  • 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
稀释度
应用 稀释度 推荐种属
FCM 5 μl per million cells in 100μl volume Ms
背景介绍
  • Ly-6C, also known as lymphocyte antigen 6 complex, is a cell surface glycoprotein that is widely used to identify functionally distinct murine circulating monocyte populations. It plays a critical role in the immune system, particularly in the activation and regulation of macrophages and monocytes. Ly-6C is expressed on various cells, including macrophages, dendritic cell precursors, granulocytes, and subsets of B- and T-lymphocytes. It is often used as a marker to differentiate between classical monocytes (Ly-6Chi) and non-classical monocytes (Ly-6Clo). In the context of tissue repair and fibrosis, Ly-6C expression has been shown to be important for identifying macrophage subsets that mediate tissue remodeling. Moreover, Ly-6C has been used as a marker for studying vascular changes in health and disease. It has been shown to be a useful marker for visualizing the retinal vasculature in mice, and its expression can be used to assess vascular changes in response to injury such as retinal ischemia.

  • 流式分析

    • Flow cytometric analysis of Mouse Ly-6C expression on C57BL/6 mouse bone marrow. C57BL/6 mouse bone marrow was stained with Brilliant Violet 421™ Rat Anti-Mouse CD11b antibody and either PE-Cy7 Rat IgG2c, κ Isotype Control (Left panel) or SDT PE-Cy7 Rat Anti-Mouse Ly-6C Antibody (Right panel) at 0.25 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.