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Invivo anti-Mouse I-A/I-E Recombinant mAb

Invivo anti-Mouse I-A/I-E Recombinant mAb

Catalog Number: S0B7082 Application: FCM Reactivity: Mouse Conjugation: Unconjugated Brand: Starter
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Regular price $170 USD
Regular price Sale price $170 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 Rat IgG2b,k
Application FCM, Functional assays, in vivo MHC II blockade
Reactivity Ms
Positive Sample C57BL/6 mouse splenocytes
Purification Protein G
Concentration 5 mg/ml
Purity >95% (Determined by SDS-PAGE)
Endotoxin <1EU/mg
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS pH7.4, containing no preservative

Stability & Storage

2 to 8 °C for 2 weeks under sterile conditions;
-20 °C for 3 months under sterile conditions;
-80 °C for 24 months under sterile conditions.
Please avoid repeated freeze-thaw cycles.

Dilution


application dilution species
FCM 1:500 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 C57BL/6 mouse splenocytes labeled with mouse I-A/I-E antibody at 1/500 dilution (1 μg) / (right panel) compared with a Rat IgG2b, κ Isotype Control / (left panel). Goat Anti-Rat IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD19 - Brilliant Violet 421™ antibody separately. Total viable cells, as determined by Fixable Viability Dye 662 (S0B88806), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.