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Alexa Fluor® 647 Rat Anti-Mouse/Human CD49f Antibody (S-R707)

Alexa Fluor® 647 Rat Anti-Mouse/Human CD49f Antibody (S-R707)

货号: S0B5139
价格: 650
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD49f
  • 分子别名

    Integrin alpha-6; CD49 antigen-like family member F; VLA-6; ITGA6
  • 细胞定位

    Cell membrane
  • Accession

    P23229, Q61739
  • 克隆号

    S-R707
  • 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

    Human peripheral blood lymphocytes
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 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 Hu, Ms
背景介绍
  • CD49f, also known as integrin α6 subunit, is a type I transmembrane glycoprotein encoded by the ITGA6 gene. It belongs to the α-subfamily of integrins and can form heterodimers with β1 (CD29) or β4 (CD104) subunits to create functional receptors such as α6β1 or α6β4. These receptors play crucial roles in cell adhesion, migration, and signaling. CD49f is highly expressed in various cell types, including T cells, monocytes, platelets, epithelial cells, and certain stem cells. In cancer biology, CD49f has been identified as a marker for tumor-initiating cells (TICs) in hepatocellular carcinoma (HCC), where it is associated with cell stemness, immune evasion, and the formation of an immunosuppressive tumor microenvironment. Additionally, CD49f has been used as a marker for human astrocytes and has shown potential in studying neurodegenerative diseases.

  • 流式分析

    • Flow cytometric analysis of CD49f expression on human peripheral blood lymphocytes. Human peripheral blood lymphocytes were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 Antibody and either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse/Human CD49f Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.