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APC Rat Anti-Mouse CD206 (MMR)Antibody (S-R498)

Macrophage mannose receptor 1,Mrc1

价格 900.00 供应商现货 : 3-5个工作日
货号 S0B80088
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD206 (MMR)
  • 分子别名

    Macrophage mannose receptor 1; Mrc1
  • 细胞定位

    Cell membrane
  • Accession

    Q61830
  • 克隆号

    S-R498
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse peritoneal exudates cells
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    APC
  • 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

    ICFCM

  • 稀释度

    应用 稀释度 推荐种属
    ICFCM 0.25μg per million cells in 100μl volume Ms
背景介绍
  • CD206, also known as the mannose receptor (MR) or mannose receptor C type 1 (MRC1), is a transmembrane glycoprotein that belongs to the C-type lectin family. It is predominantly expressed by tissue macrophages, dendritic cells, and certain lymphatic or liver endothelial cells. CD206 recognizes and mediates endocytosis of pathogens by binding to glycoproteins terminated with mannose. This receptor serves as a homeostatic receptor by binding and scavenging unwanted high mannose N-linked glycoproteins as well as pituitary hormones from the circulation. In addition, CD206 is a marker for the M2 phenotype of macrophages, which are involved in immunosuppression, tissue remodeling, and Th2 effector responses. Its expression is regulated by various cytokines and is considered a marker of an M2-like macrophage phenotype.

  • 流式分析

    • Flow cytometric analysis of mouse CD206 (MMR) expression on 4% paraformaldehyde fixed and 0.1% Tween permeabilized BALB/c mouse peritoneal exudates cells. The cells were then stained with Pacific Blue™ Rat Anti-Mouse F4/80 Antibody and either APC Rat IgG2a, κ Isotype Control (left panel) or SDT APC Rat Anti-Mouse CD206 (MMR) Antibody (right panel) at 1.25 μl/test. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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