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  • 二抗
  • 慢病毒
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Anti-CD8a Rabbit Monoclonal Antibody #50107

一键复制产品信息
Immunohistochemical analysis of CD8a staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
  • 基因名:
    CD8A
  • 货号:
    50107
  • 应用:
    IHC
  • 物种反应性:
    H
规格:
20 μL,50 μL,100 μL
价格:
¥ 560.00,¥ 1,100.00,¥ 2,000.00
Information
Product Name Anti-CD8a Rabbit Monoclonal Antibody
Aliases MAL; T-cell surface glycoprotein CD8 alpha chain; T-lymphocyte differentiation antigen T8/Leu-2; CD8a
Background

Gene Name: CD8A

NCBI Gene Entry: 925

UniProt Entry: P01732

Application Information

Molecular Weight: Predicted, 26 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB8425

Species Reactivity: Human

Applications Tested: Immunohistochemistry (IHC)

Immunogen Recombinant protein of human CD8a
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.3) containing 50% glycerol, and 0.05% Proclin300.
Storage Store at -20 °C for one year.
Recommended Dilutions Immunohistochemistry (IHC): 1:100-1:200
Note This product is for research use only.
Picture
  • Immunohistochemical analysis of CD8a staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Citation(0)
Immunohistochemical analysis of CD8a staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
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