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APC-Cy7 Rat Anti-Mouse I-A/I-E Antibody (S-R511)

APC-Cy7 Rat Anti-Mouse I-A/I-E Antibody (S-R511)

Catalog Number: S0B5464 Application: FCM Reactivity: Mouse Conjugation: APC-Cy7 Brand: Starter
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Regular price $200 USD
Regular price Sale price $200 USD
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Product Details

Product Specification


Host Rat
Antigen I-A/I-E
Synonyms H-2 class II histocompatibility antigen, I-A beta chain; H2-Eb1
Location Membrane
Accession P18468、 Q3U060
Clone Number S-R511
Antibody Type Rat mAb
Isotype IgG2b,k
Application FCM
Reactivity Ms
Positive Sample BALB/c mouse splenocytes
Purification Protein G
Concentration 0.05mg/ml
Conjugation APC-Cy7
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 Ms

Background

I-A/I-E proteins are part of the Major Histocompatibility Complex (MHC) class II molecules, which are heterodimeric transmembrane glycoproteins expressed on antigen-presenting cells such as dendritic cells, macrophages, and B cells. These proteins are encoded by four genes located in the mouse MHC and are composed of α and β subunits. The I-A and I-E molecules are highly polymorphic and can form hybrid molecules in heterozygous individuals, contributing to the diversity of antigen presentation. They play a crucial role in presenting peptide antigens to CD4+ helper T cells, initiating adaptive immune responses. Additionally, MHC class II molecules can trigger intracellular signaling pathways in antigen-presenting cells, influencing their proliferation, maturation, and apoptosis.

Picture

FC

Flow cytometric analysis of Mouse I-A/I-E expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Alexa Fluor® 647 Rat Anti-Mouse CD19 antibody and either APC-Cy7 Rat IgG2b, κ Isotype Control (Left panel) or SDT APC-Cy7 Rat Anti-Mouse I-A/I-E antibody (Right panel) at 5 μl/test treated with True-Stain Monocyte Blocker™. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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