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Biotin Rabbit Anti-Mouse NK1.1/CD161 Antibody (S-428-32)

Biotin Rabbit Anti-Mouse NK1.1/CD161 Antibody (S-428-32)

货号: S0B5088
价格: 300
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; Ly55c; Nkrp1c; 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

    Biotin
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, 0.03% 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
  • NK1.1/CD161, also known as KLRB1 or NKR-P1A, is a type II transmembrane C-type lectin-like receptor expressed as a disulfide-linked homodimer on the cell membrane. It is predominantly found on the majority of natural killer (NK) cells and subsets of peripheral T cells, including both CD4+ and CD8+ T cells, particularly those with a "memory" antigenic phenotype. The expression of CD161 is specifically upregulated by IL-12 and is associated with the cytotoxic function of CD16+ NK cells. Functionally, CD161 plays a role in modulating the activation and proliferation of NK cells, inducing interferon-γ production, and releasing cytotoxic granules. When CD161 binds to its ligand LLT1, it inhibits NK cell cytotoxicity and cytokine secretion.

  • 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 Phycoerythrin Rat Anti-Mouse CD49b Antibody and either Biotin Isotype Control (Left panel) or SDT Biotin Rabbit Anti-Mouse NK1.1/CD161 Antibody (Right panel) at 5μl/test followed by Sav-iFluor 488. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.