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Alexa Fluor® 647 Rat Anti-Mouse CD204 Antibody (S-R712)

Alexa Fluor® 647 Rat Anti-Mouse CD204 Antibody (S-R712)

货号: S0B5447
价格: 500
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD204
  • 分子别名

    Macrophage scavenger receptor types I and II; Macrophage acetylated LDL receptor I and II; Scavenger receptor type A (SR-A); Scvr; Msr1
  • Accession

    P30204
  • 克隆号

    S-R712
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse peritoneal exudates cells
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 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 5μl per million cells in 100μl volume Ms
背景介绍
  • CD204, also known as macrophage scavenger receptor 1 (MSR1) or scavenger receptor A (SR-A), is a class A scavenger receptor primarily expressed on macrophages and dendritic cells. It functions as a pattern recognition receptor that binds to a wide range of polyanionic ligands, such as modified lipid proteins and pathogen-derived molecules. CD204 plays roles in lipid metabolism, atherogenesis, and various metabolic processes. It is also involved in innate defense against pathogens and has been implicated in several diseases, including Alzheimer's disease. In cancer, CD204 is a specific marker of tumor-associated macrophages (TAMs) and is associated with poor prognosis in glioma and breast cancer. Additionally, CD204+ monocytes and macrophages can suppress proinflammatory cytokine production and protect mice from septic shock.

  • 流式分析

    • Flow cytometric analysis of Mouse CD204 expression on BALB/c mouse peritoneal exudates cells. BALB/c mouse peritoneal exudates cells were stained with SDT FITC Rat Anti-Mouse F4/80 Antibody (S0B5113) at 5 μl/test and either Alexa Fluor® 647 Rat IgG2b, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse CD204 Antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.