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Alexa Fluor® 647 Mouse anti-Human CD8 Antibody (S-R533)

Alexa Fluor® 647 Mouse anti-Human CD8 Antibody (S-R533)

Catalog Number: S0B5802 Application: FCM Reactivity: Human Conjugation: Alexa Fluor® 647 Brand: Starter
Price:
Regular price $120 USD
Regular price Sale price $120 USD
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Product Details

Product Specification


Host Mouse
Antigen CD8α
Synonyms T-cell surface glycoprotein CD8 alpha chain; T-lymphocyte differentiation antigen T8/Leu-2; MAL; CD8A
Location Cell membrane
Accession P01732
Clone Number S-R533
Antibody Type Mouse mAb
Isotype IgG1
Application FCM
Reactivity Hu
Positive Sample human peripheral blood lymphocytes
Purification Protein G
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 647
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 1.25μl per million cells in 100μl volume Hu

Background

CD8α is a crucial immune glycoprotein that plays a vital role in the immune response by serving as a co-receptor for the T-cell receptor (TCR) on cytotoxic T cells. It forms either a homodimer (α/α) or a heterodimer with CD8β (α/β) to interact with MHC class I molecules on antigen-presenting cells (APCs), facilitating the recognition of intracellular pathogens such as viruses. CD8α also recruits the LCK kinase, which initiates downstream signaling pathways essential for T-cell activation and proliferation. This molecule is critical for the function of cytotoxic T lymphocytes (CTLs) and is involved in various immune-related diseases, including immunodeficiencies and autoimmune conditions.

Picture

FC

Flow cytometric analysis of Human CD8 expression on human peripheral blood lymphocytes. Human peripheral blood lymphocytes were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody and either Alexa Fluor® 647 Mouse IgG1 Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti- Human CD8 antibody (Right panel) at 1.25 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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