Fig. 2.
Fig. 2. Activated NF-κB measured by flow cytometry in human CD4+ peripheral T cells ([A] unstimulated, [B] stimulated) and CD34+CD19− bone marrow cells ([C] unstimulated, [D] stimulated). Stimulated cells were incubated with 25 ng/mL PMA and 1 μg/mL ionomycin for 1 hour at 37°C before NF-κB analysis. Activated NF-κB is a black line and the background isotype antibody binding is a gray line for each sample. The monoclonal antibody used in these experiments has been shown to be specific for the NF-κB nuclear localization region, which is detected only if NF-κB is activated. The CD4+ T cells and CD34+CD19− bone marrow cells were more than 97% and more than 99% pure, respectively.

Activated NF-κB measured by flow cytometry in human CD4+ peripheral T cells ([A] unstimulated, [B] stimulated) and CD34+CD19 bone marrow cells ([C] unstimulated, [D] stimulated). Stimulated cells were incubated with 25 ng/mL PMA and 1 μg/mL ionomycin for 1 hour at 37°C before NF-κB analysis. Activated NF-κB is a black line and the background isotype antibody binding is a gray line for each sample. The monoclonal antibody used in these experiments has been shown to be specific for the NF-κB nuclear localization region, which is detected only if NF-κB is activated. The CD4+ T cells and CD34+CD19 bone marrow cells were more than 97% and more than 99% pure, respectively.

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