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Hladr g46 6 apc h7

Manufactured by BD

HLADR (G46-6) APC-H7 is a monoclonal antibody product designed for flow cytometry applications. It is used to identify and characterize human leukocyte antigen DR (HLA-DR) expression on cells. The APC-H7 fluorochrome conjugated to the antibody allows for multicolor flow cytometry analysis.

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2 protocols using hladr g46 6 apc h7

1

Multiparametric Cytometry of Immune Cells

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Polychromatic flow cytometry and cell sorting were performed on stained mononuclear cells utilizing the BD LSRFortessa and FACS Aria, respectively, equipped with FACS DiVA software. The following Abs were used for staining at predetermined concentrations: CD3 (clone SP34-2) AL700, HLADR (G46-6) APC-H7, IL-2 (MQ1-17H12) FITC, and Ki67 (B56) FITC from BD; CD4 (OKT4) eFluor450, CD8 (SK1) PerCP-e710, IFNg (4S.B3) eFluor450, IL17A (eBio64DEC17) PE, IL22 (IL22JOP) APC, and TNFa (MAb11) PE-Cy7 from eBioscience; CD28 (CD28.2) ECD from Beckman Coulter; and CD95 (DX2) PE-Cy5 from Biolegend. Cell viability was assessed using the Live/Dead Aqua Fixable Dead Cell Stain (Invitrogen). Cells were permeabilized with Cytofix/Cytoperm (BD) prior to intracellular staining. Acquired data were analyzed using FlowJo software. To quantify cell subset frequencies, we used a threshold cutoff of 100 cells of the parent population. For TH17 functional analyses, cytokine gates were established on a threshold cutoff of 100 CD4+ or CD8+ TM and Boolean gates utilized to ascertain frequencies – populations not meeting this threshold were not considered for analysis.
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2

Multiparametric Cytometry of Immune Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Polychromatic flow cytometry and cell sorting were performed on stained mononuclear cells utilizing the BD LSRFortessa and FACS Aria, respectively, equipped with FACS DiVA software. The following Abs were used for staining at predetermined concentrations: CD3 (clone SP34-2) AL700, HLADR (G46-6) APC-H7, IL-2 (MQ1-17H12) FITC, and Ki67 (B56) FITC from BD; CD4 (OKT4) eFluor450, CD8 (SK1) PerCP-e710, IFNg (4S.B3) eFluor450, IL17A (eBio64DEC17) PE, IL22 (IL22JOP) APC, and TNFa (MAb11) PE-Cy7 from eBioscience; CD28 (CD28.2) ECD from Beckman Coulter; and CD95 (DX2) PE-Cy5 from Biolegend. Cell viability was assessed using the Live/Dead Aqua Fixable Dead Cell Stain (Invitrogen). Cells were permeabilized with Cytofix/Cytoperm (BD) prior to intracellular staining. Acquired data were analyzed using FlowJo software. To quantify cell subset frequencies, we used a threshold cutoff of 100 cells of the parent population. For TH17 functional analyses, cytokine gates were established on a threshold cutoff of 100 CD4+ or CD8+ TM and Boolean gates utilized to ascertain frequencies – populations not meeting this threshold were not considered for analysis.
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