您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
PerCP-Cy5.5 Rabbit Anti-Mouse NK1.1/CD161 Antibody (S-428-32)

PerCP-Cy5.5 Rabbit Anti-Mouse NK1.1/CD161 Antibody (S-428-32)

货号: S0B1730
价格: 1500
规格: 50T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    NK1.1/CD161
  • 分子别名

    Killer cell lectin-like receptor subfamily B member 1C; CD161 antigen-like family member C; Lymphocyte antigen 55c (Ly-55c); NKR-P1.9; NKR-P1C; Natural killer cell surface protein P1-40 (NKR-P1 40); CD161c; Klrb1c
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Membrane
  • Accession

    P27814
  • 克隆号

    S-428-32
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein A
  • 浓度

    0.2 mg/ml
  • 标记

    PerCP-Cy5.5
  • 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
  • CD161 is a C-type lectin-like membrane receptor expressed at high levels on NK, NKT, Th17, Mucosa Associated Invariant T cells (MAITs), non-MAIT CD8+, tissue-resident memory cells (TRMs), αβ CD4+ T cells and CD8+ T cells. CD161 levels increase when αβ T cells enter tissues. The ligand for CD161 is the lectin-like transcript 1 (LLT1). CD161/LLT1 engagement inhibits NK cell function but can inhibit or enhance αβ T cell function depending on the co-stimulatory molecules involved. The inhibitory capacity of αβ T cells can be neutralized by blocking CD161. CD161 expression on γδ T cells is associated with enhanced IFN-γ and IL-17 production and enhanced endothelial transmigration.

  • 流式分析

    • Flow cytometric analysis of Mouse NK1.1/CD161 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Alexa Fluor® 488 Rat Anti-Mouse CD49b antibody and either PerCP-Cy5.5 Rabbit IgG Isotype Control (Left panel) or SDT PerCP-Cy5.5 Rabbit Anti-Mouse NK1.1/CD161 Antibody (Right panel) at 1 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.