• 一抗
  • 二抗
  • 慢病毒
  • 细胞系
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Anti-CD134 Rabbit Monoclonal Antibody #50112

一键复制产品信息
Immunohistochemical analysis of CD134 staining in human tonsil 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:
    TNFRSF4
  • 货号:
    50112
  • 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-CD134 Rabbit Monoclonal Antibody
Aliases TXGP1L; Tumor necrosis factor receptor superfamily member 4; ACT35 antigen; OX40L receptor; TAX transcriptionally-activated glycoprotein 1 receptor; CD134
Background

Gene Name: TNFRSF4

NCBI Gene Entry: 7293

UniProt Entry: P43489

Application Information

Molecular Weight: Predicted, 29 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB8450

Species Reactivity: Human

Applications Tested: Immunohistochemistry (IHC)

Immunogen Recombinant protein of human CD134
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 CD134 staining in human tonsil 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 CD134 staining in human tonsil 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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