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Il 2 apc mq1 17h12

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IL-2 APC (MQ1-17H12) is a fluorescently-labeled antibody that binds to the interleukin-2 (IL-2) protein. It is commonly used in flow cytometry applications to detect and quantify IL-2 expression in biological samples.

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2 protocols using il 2 apc mq1 17h12

1

Multiparameter Flow Cytometry for Cytokine Profiling

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Cell staining was performed on cryopreserved fixed cells that were thawed and washed with 1% FACS washing buffer (1% FBS in PBS). Cells were stained with the following surface antibody markers: CD4 ECD (SFCI12T4D11, Beckman Coulter), CD8 BV510 (RPA-8, Biolegend) and incubated at room temperature for 20 minutes. Cells were permeabilized and stained with intracellular antibody markers CD3 BV650 (OKT3), IFN-γ AlexaFluor® 700 (B27), TNF-α BV786 (Mab11) and IL-2 APC (MQ1-17H12) (all from Biolegend). Finally, cells were washed and fixed with Cellfix (BD Biosciences). Samples were acquired on a multiparameter BD Fortessa flow cytometer using Diva software version 8 and analyzed using FlowJo v10. Results are expressed as the frequency of CD4+ or CD8+ T cells expressing IFN-γ, TNF-α or IL-2. Cytokine responses presented are background subtracted values (from the frequency of cytokine produced by unstimulated cells).
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2

Cryopreserved Cell Staining for Cytokine Analysis

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Cell staining was performed on cryopreserved fixed cells that were thawed and washed with 1% FACS washing buffer (1% FBS in PBS). A viability dye was not included during the staining process, as it has been reported that the omission of a viability dye during the staining process does not impact the detection and quantification of cytokines when using the whole blood-based T cell assay.88 (link) Cells were stained with the following surface antibody markers: CD4 ECD (SFCI12T4D11, Beckman Coulter), CD8 BV510 (RPA-8, Biolegend) and incubated at room temperature for 20 min. Cells were permeabilized and stained with intracellular antibody markers CD3 BV650 (OKT3), IFN-γ AlexaFluor 700 (B27), TNF-α BV786 (Mab11) and IL-2 APC (MQ1-17H12) (all from Biolegend). Finally, cells were washed and fixed with Cellfix (BD Biosciences). Samples were acquired on a multiparameter BD Fortessa flow cytometer using Diva software version 9 and analyzed using FlowJo v10. Results are expressed as the frequency of CD4+ or CD8+ T cells expressing IFN-γ, TNF-α or IL-2. Cytokine responses presented are background subtracted values (from the frequency of cytokine produced by unstimulated cells).
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