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FITC Syrian hamster Anti-Mouse Podoplanin Antibody (S-R689)

Glycoprotein 38,OTS-8,PA2.26 antigen,Transmembrane glycoprotein E11,Gp38,Ots8,Pdpn

价格 900.00 1-2周
货号 S0B5163
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Syrian Hamster
  • 抗原名称

    Podoplanin
  • 分子别名

    Glycoprotein 38; OTS-8; PA2.26 antigen; Transmembrane glycoprotein E11; Gp38; Ots8; Pdpn
  • 细胞定位

    Cell membrane
  • Accession

    Q62011
  • 克隆号

    S-R689
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Ms
  • 阳性样本

    C2C12. Cells
  • 纯化方式

    Protein G
  • 浓度

    0.05mg/ml
  • 标记

    FITC
  • 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 5μl per million cells in 100μl volume Ms
背景介绍
  • Podoplanin is a small, mucin-like transmembrane glycoprotein that plays diverse roles in both physiological and pathological processes. Initially identified in podocytes of the kidney, it is also expressed in various tissues, including the brain, heart, lungs, and lymphatic endothelium. Podoplanin is a key marker for lymphatic vessels and is involved in lymphangiogenesis, embryonic development, and platelet aggregation. In cancer, its expression is associated with tumor invasion and metastasis, making it a potential therapeutic target. Additionally, podoplanin has been implicated in neurological disorders, inflammation, and immune responses, highlighting its multifaceted importance in health and disease.

  • 流式分析

    • Flow cytometric analysis of Mouse Podoplanin expression on C2C12. Cells from the C2C12 (Mouse myoblasts myoblast, Right) or RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage, Left) was stained with either FITC Syrian hamster IgG Isotype Control (Black line histogram) or SDT FITC Syrian hamster Anti-Mouse Podoplanin Antibody (Red line histogram) at 5μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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