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FITC Rat Anti-Mouse CD16/CD32 Antibody (2.4G2)

Low affinity immunoglobulin gamma Fc region receptor III,IgG Fc receptor III,Fc-gamma RIII (FcRIII),Fcgr3,Low affinity immunoglobulin gamma Fc region receptor II,Fc gamma receptor IIB,Fc-gamma RII,Fc-gamma-RIIB,FcRII,IgG Fc receptor II beta,Lymphocyte antigen 17 (Ly-17),Fcgr2,Fcgr2b,Ly-17

价格 500.00 供应商现货 : 3-5个工作日
货号 S0B8266
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD16/CD32
  • 分子别名

    Low affinity immunoglobulin gamma Fc region receptor III; IgG Fc receptor III; Fc-gamma RIII (FcRIII); Fcgr3; Low affinity immunoglobulin gamma Fc region receptor II; Fc gamma receptor IIB; Fc-gamma RII; Fc-gamma-RIIB; FcRII; IgG Fc receptor II beta; Lymphocyte antigen 17 (Ly-17); Fcgr2; Fcgr2b; Ly-17
  • 细胞定位

    Cell membrane
  • Accession

    P08508, P08101
  • 克隆号

    2.4G2
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    FITC
  • 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 5μl per million cells in 100μl volume Ms
背景介绍
  • CD16/CD32 proteins, also known as FcγRIII and FcγRII, are cell surface receptors expressed on immune cells such as natural killer cells, macrophages, and certain T cell subsets; they bind the Fc region of immunoglobulin G to mediate antibody-dependent cellular cytotoxicity, phagocytosis, and immune complex clearance by triggering activating (ITAM-based) or inhibitory (ITIM-based) signaling cascades that modulate innate and adaptive immune responses.

  • 流式分析

    • Flow cytometric analysis of CD16/CD32 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with either FITC Rat IgG2b, κ Isotype Control (Black line histogram) or SDT FITC Rat Anti-Mouse CD16/CD32 antibody (Red line histogram) at 5 μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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