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APC Rat Anti-Mouse MERTK Antibody (S-R603)

APC Rat Anti-Mouse MERTK Antibody (S-R603)

货号: S0B5141
价格: 845
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    MERTK
  • 分子别名

    Tyrosine-protein kinase Mer; Proto-oncogene c-Mer; Receptor tyrosine kinase MerTK; Mer; Mertk
  • 细胞定位

    Cell membrane
  • Accession

    Q60805
  • 克隆号

    S-R603
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse peritoneal exudates cells
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    APC
  • 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 5μl per million cells in 100μl volume Ms
背景介绍
  • MERTK, also known as MER proto-oncogene tyrosine kinase, is a receptor tyrosine kinase and a member of the TAM (TYRO3, AXL, MERTK) family. It plays crucial roles in various physiological processes, including cell survival, migration, differentiation, and the phagocytosis of apoptotic cells, a process known as efferocytosis. MERTK is expressed in multiple tissues, such as macrophages and retinal pigment epithelial cells, and is involved in regulating immune responses and maintaining tissue homeostasis. In the immune system, MERTK helps macrophages clear apoptotic cells and inhibits the innate immune response by activating STAT1, which induces the production of suppressors of cytokine signaling (SOCS1 and SOCS3). Abnormal expression of MERTK has been linked to several diseases, including retinitis pigmentosa and certain cancers, making it a potential therapeutic target in cancer treatment.

  • 流式分析

    • Flow cytometric analysis of Mouse MERTK expression on C57BL/6 mouse peritoneal exudates cells. C57BL/6 mouse peritoneal exudates cells were stained with FITC Rat Anti-Mouse F4/80 Antibody (S0B5113) at 5μl/test and either APC Rat IgG2a, κ Isotype Control (Left panel) or SDT APC Rat Anti-Mouse MERTK Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.