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Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
A: | B: |
FoxP3 Staining Buffer SetFigure 1Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. | FoxP3 Staining Buffer SetFigure 1Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
A: | B: |
FoxP3 Staining Buffer SetFigure 2Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. | FoxP3 Staining Buffer SetFigure 2Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
A: | B: |
FoxP3 Staining Buffer SetFigure 1Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. | FoxP3 Staining Buffer SetFigure 1Human PBMCs were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
A: | B: |
FoxP3 Staining Buffer SetFigure 2Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. | FoxP3 Staining Buffer SetFigure 2Mouse splenocytes were stained with CD4-FITC. Cells were fixed, permeabilized, and intracellularly stained with Anti-FoxP3-PE (A) or Anti-FoxP3-APC (B) using the FoxP3 Staining Buffer Set. Cells were analyzed by flow cytometry. |
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