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Alexa Fluor® 700 Rat Anti-Mouse CD8α Antibody (S-353-45)

Alexa Fluor® 700 Rat Anti-Mouse CD8α Antibody (S-353-45)

Catalog Number: S0B1662 Application: FCM Reactivity: Mouse Conjugation: Alexa Fluor 700 Brand: Starter
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Regular price $110 USD
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Product Details

Product Specification


Host Rat
Antigen CD8α
Synonyms Lyt-2
Immunogen Recombinant Protein
Location Cell membrane
Accession P01731
Clone Number S-353-45
Antibody Type Rat mAb
Isotype IgG1,λ
Application FCM
Reactivity Ms
Positive Sample BALB/c mouse splenocytes
Purification Protein G
Concentration 0.1mg/ml
Conjugation Alexa Fluor® 700
Physical Appearance Liquid
Storage Buffer PBS, 25% Glycerol, 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 5 μl per million cells in 100μl volume Ms

Background

CD8a, also known as CD8α, is a molecular marker on the surface of T lymphocytes. It belongs to the family of leukocyte differentiation antigens and is primarily expressed on the surface of cytotoxic T lymphocytes (CTLs). CD8a plays a crucial role in immune responses related to cytotoxicity and local inflammation. It has the ability to bind to MHC class I molecules. The expression level of CD8 molecules undergoes changes during various stages of T cell differentiation, development, and in response to T cell stimuli. Additionally, CD8a is closely associated with autoimmune monitoring, humoral immune responses, and transplant reactions. For instance, CD8a can serve as a monitoring indicator for certain autoimmune diseases and plays a significant role in immunotherapy for anti-tumor and anti-viral treatments.

Picture

FC

Multiparameter flow cytometric analysis of Mouse CD8α expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 antibody and either Alexa Fluor® 700 Mouse IgG1, λ Isotype Control (Left panel) or SDT Alexa Fluor® 700 Rat Anti- Mouse CD8α antibody (Right panel) at 0.5 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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