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Alexa Fluor® 488 Mouse Anti-Human CD7 Antibody (S-575-17)

T-cell antigen CD7,GP40,T-cell leukemia antigen,T-cell surface antigen Leu-9,TP41

价格 847.00 供应商现货 : 3-5个工作日
货号 S0B8657
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD7
  • 分子别名

    T-cell antigen CD7; GP40; T-cell leukemia antigen; T-cell surface antigen Leu-9; TP41
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cell membrane
  • Accession

    P09564
  • 克隆号

    S-575-17
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 阳性样本

    human peripheral blood leukocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    Alexa Fluor® 488
  • 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

  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1.25 μl per million cells in 100μl volume Hu
背景介绍
  • CD7, also known as GP40, is a transmembrane glycoprotein and a member of the immunoglobulin superfamily, primarily expressed on the surface of T cells and natural killer (NK) cells. It is highly expressed in acute T-cell leukemia (T-ALL) and certain peripheral T-cell lymphomas. CD7 plays a significant role in the regulation and activation of the immune system. It is involved in T-cell and T-cell/B-cell interactions during early lymphoid development and acts as a co-stimulatory molecule with CD3, CD45, and PI3K. CD7 has two known ligands, K12 protein and galectin-1, which can influence T cell proliferation, migration, and apoptosis. Additionally, CD7 is being explored as a target for cancer therapies, such as antibody-drug conjugates, due to its high expression in certain malignancies.

  • 流式分析

    • Flow cytometric analysis of human CD7 expression on human peripheral blood leukocytes. Human peripheral blood leukocytes were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody and either Alexa Fluor® 488 mouse IgG1, κ Isotype Control (left panel) or SDT Alexa Fluor® 488 Mouse Anti-Human CD7 antibody (right panel) at 1.25 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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