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PerCP-Cy5.5 Mouse Anti-Human CD103 Antibody (S-2876)

PerCP-Cy5.5 Mouse Anti-Human CD103 Antibody (S-2876)

Catalog Number: S0B5942 Application: FCM Reactivity: Human Conjugation: PerCP-Cy5.5 Brand: Starter
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Regular price $294.00 SGD
Regular price Sale price $294.00 SGD
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Product Details

Product Specification


Host Mouse
Antigen CD103
Synonyms Integrin alpha-E; HML-1 antigen; Integrin alpha-IEL; Mucosal lymphocyte 1 antigen; ITGAE
Location Membrane
Accession P38570
Clone Number S-2876
Antibody Type Mouse mAb
Isotype IgG1,k
Application FCM
Reactivity Hu
Positive Sample Human PBMC
Purification Protein G
Concentration 0.2 mg/ml
Conjugation PerCP-Cy5.5
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
FCM 5μl per million cells in 100μl volume Hu

Background

CD103, also known as integrin αEβ7, is a transmembrane heterodimer complex primarily expressed on tissue-resident memory T cells (T RM cells), regulatory T cells (Tregs), and certain dendritic cells. It binds to E-cadherin on epithelial cells, mediating lymphocyte adhesion and retention in tissues such as the skin, gut, and lungs. This interaction is crucial for immune surveillance and maintaining tissue integrity. CD103 expression is regulated by TGF-β, which enhances its ability to bind E-cadherin. In cancer research, CD103 is significant in tumor-infiltrating lymphocytes (TILs), influencing immune responses within tumors. Additionally, CD103 plays a role in cytotoxic T cell activation and effective tumor cell lysis.

Picture

FC

Flow cytometric analysis of Human CD103 expression on Human PBMC. Human PBMC (peripheral blood mononuclear cells) were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 Antibody and either Percp-Cy5.5 Mouse IgG1, κ Isotype Control (Left panel) or Percp-Cy5.5 Mouse Anti-Human CD103 Antibody (Right panel) at 5 μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 662 (S0D0016), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.