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Pe anti human cd223 lag 3 antibody

Manufactured by BioLegend

The PE anti-human CD223 (LAG-3) antibody is a fluorochrome-conjugated monoclonal antibody that specifically binds to the CD223 (also known as LAG-3) cell surface receptor on human cells. CD223 is an inhibitory receptor that plays a role in the regulation of T cell activation and function.

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2 protocols using pe anti human cd223 lag 3 antibody

1

Characterization of Immune Cell Subsets in PBMCs

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Peripheral blood mononuclear cells (PBMCs) were isolated from blood samples using a Ficoll gradient (Axis Shield, Norway). Unstimulated PBMCs were stained with APC anti-human CD19 antibody (BioLegend cat #302212), APC/Cyanine7 anti-human CD138 antibody (BioLegend cat #356528), PerCP/Cyanine5.5 anti-human CD1d antibody (BioLegend cat #350312), APC anti-human CD25 antibody (BioLegend cat #302610), and PE anti-human CD223 (LAG-3) antibody (BioLegend cat #369306). After surface staining, cells were stained with PE anti-human EBi3 antibody (BioLegend cat #360904) and PE/Cy7 anti-human IL-10 antibody (BioLegend cat #501420), FITC anti-human FOXP3 antibody (BioLegend cat #320106). Corresponding isotype controls were used for each antibody. All cells were analyzed with BD LSR II flow cytometer using DIVA software version 8.0.
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2

Phenotypic Characterization of PBMCs

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Isolation of peripheral blood mononuclear cells (PBMCs) was performed using a Ficoll gradient (Axis-Shield, Norway). The unstimulated PBMCs were stained with APC anti-human CD19 antibody (BioLegend cat #302212), APC/Cyanine7 anti-human CD138 antibody (BioLegend cat #356528), PerCP/Cyanine5.5 anti-human CD1d antibody (BioLegend cat #350312), APC anti-human CD25 antibody (BioLegend cat #302610), and PE anti-human CD223 (LAG-3) antibody (BioLegend cat #369306). Following surface staining, cells were stained with PE anti-human EBi3 antibody (BioLegend cat #360904), PE/Cy7 anti-human IL-10 antibody (BioLegend cat #501420), and FITC anti-human FOXP3 antibody (BioLegend cat #320106). For each antibody, the corresponding isotype controls were used. All cells were analyzed with BD LSR II flow cytometer using DIVA software version 8.0.
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