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PerCP-Cy5.5 Rat Anti-Mouse CD335/NKP46 Antibody (S-R613)

Natural cytotoxicity triggering receptor 1,Activating receptor 1 (mAR-1),Lymphocyte antigen 94,Natural killer cell p46-related protein (NK-p46,NKp46,mNKp46),Ly94,Ncr1

价格 500.00 1-2周
货号 S0B80558
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD335
  • 分子别名

    Natural cytotoxicity triggering receptor 1; Activating receptor 1 (mAR-1); Lymphocyte antigen 94; Natural killer cell p46-related protein (NK-p46; NKp46; mNKp46); Ly94; Ncr1
  • 细胞定位

    Cell membrane
  • Accession

    Q8C567
  • 克隆号

    S-R613
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,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

    PerCP-Cy5.5
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.09% sodium azide

  • 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 1μg per million cells in 100μl volume Ms
背景介绍
  • CD335, also known as NKp46 or Natural Cytotoxicity Triggering Receptor 1 (NCR1), is a 46 kDa type I transmembrane glycoprotein that belongs to the natural cytotoxicity receptor family. It is primarily expressed on natural killer (NK) cells and plays a crucial role in their activation and cytotoxicity. CD335 can recognize and bind to viral hemagglutinins and heparan sulfate proteoglycans on target cells, triggering NK cell-mediated cytotoxic responses. This receptor is involved in non-MHC-restricted natural cytotoxicity and is essential for the immune system's ability to detect and eliminate infected or transformed cells.

  • 流式分析

    • Flow cytometric analysis of CD335 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Alexa Fluor® 647 Mouse Anti-Mouse NK1.1 antibody (S0B5488) and either PerCP-Cy5.5 Rat IgG2a, κ Isotype Control (left panel) or SDT PerCP-Cy5.5 Rat Anti-Mouse CD335 Antibody (right panel) at 5 μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 452 (S0B88801), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.

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