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CD31 Recombinant Rabbit mAb (SDT-008-17)

PECAM-1,EndoCAM,GPIIA,PECA1

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B2009
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    CD31
  • 分子别名

    PECAM-1,EndoCAM, GPIIA, PECA1
  • 免疫原

    Synthetic Peptide
  • Accession

    P16284
  • 克隆号

    SDT-008-17
  • 抗体类型

    Rabbit mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein A
  • 研究领域

    Immunology
  • 浓度

    0.5mg/ml
  • 分子量

    150kDa

  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05%BSA, 0.03% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

  • 应用

    IHC-P ?

    WB

    IP

  • 稀释度

    应用 稀释度
    IHC-P 1:250
    IP 1:25
    WB 1:1000
背景介绍
  • Cluster of differentiation 31 (CD31) also known as platelet endothelial cell adhesion molecule (PECAM-1) is a member of the immunoglobulin superfamily and is likely involved in leukocyte transmigration, angiogenesis, and integrin activation. PECAM-1 plays a key role in removing aged neutrophils from the body. PECAM-1 is found on the surface of platelets, monocytes, neutrophils, and some types of T-cells, and makes up a large portion of endothelial cell intercellular junctions. In immunohistochemistry, CD31 is used primarily to demonstrate the presence of endothelial cells in histological tissue sections. This can help to evaluate the degree of tumor angiogenesis, which can imply a rapidly growing tumor. Malignant endothelial cells also commonly retain the antigen, so that CD31 immunohistochemistry can also be used to demonstrate both angiomas and angiosarcomas. It can also be demonstrated in small lymphocytic and lymphoblastic lymphomas, although more specific markers are available for these conditions.

  • 免疫印迹

    • WB result of anti-CD31 antibody

      Primary antibody : Anti-CD31 antibody at 1/1000 dilution
      Lane 1 : Hela whole cell lysate 20 µg
      Lane 2 : THP1 whole cell lysate 20 µg
      Negative control: Hela whole cell lysate

      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution

      Predicted MW: 82 kDa
      Observed MW: 150 kDa

  • 免疫沉淀

    • CD31 Rabbit mAb at 1/25 dilution (2µg) immunoprecipitating CD31 in 0.4mg THP-1 whole cell lysate. Western blot was performed on the immunoprecipitate using CD31 Rabbit mAb at 1/1000 dilution. Secondary antibody (HRP) for IP was used at 1/400 dilution.
      Lane 1: THP-1 whole cell lysate 10µg (input)
      Lane 2: CD31 Rabbit mAb IP in THP-1 whole cell lysate
      Lane 3: Rabbit monoclonal IgG IP in THP-1 whole cell lysate
      Predicted MW: 82 kDa
      Observed MW: 150 kDa

  • 免疫组化

    • IHC shows membrane staining in paraffin-embedded human kidney endothelial cells.

      Anti-CD31 antibody was used at 1/250 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows membrane staining in paraffin-embedded human placenta endothelial cells.

      Anti-CD31 antibody was used at 1/250 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows membrane staining in paraffin-embedded human lung squamous cell cancer endothelial cells.

      Anti-CD31 antibody was used at 1/250 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows membrane staining in paraffin-embedded human hepatocellular carcinoma endothelial cells.

      Anti-CD31 antibody was used at 1/250 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

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