Figure 3
Figure 3. Intracellular β-catenin protein levels are increased in Eμ-TCL1–induced leukemia cells. Flow staining was performed on lymphocytes isolated from the peripheral blood of tumor bearing Eμ-TCL1 mice (> 10 months old), aged WT mice (> 10 months old), and young Eμ-TCL1 mice (6 weeks old). As shown in the left panels, anti–mouse CD19-APC and CD5-phycoerythrin are used to gate CD19+CD5+ and CD19+CD5− B cells. The right panels show the fluorescence intensity of FITC-conjugated anti–β-catenin in CD19+CD5+ (dotted line) and CD19+CD5− (solid line) B-cell populations. The numbers state the net geometric mean of the fluorescence intensity (Geo Meanβ-catenin − Geo Meanisotype control). Representative data of 3 independent analyses are shown.

Intracellular β-catenin protein levels are increased in Eμ-TCL1–induced leukemia cells. Flow staining was performed on lymphocytes isolated from the peripheral blood of tumor bearing Eμ-TCL1 mice (> 10 months old), aged WT mice (> 10 months old), and young Eμ-TCL1 mice (6 weeks old). As shown in the left panels, anti–mouse CD19-APC and CD5-phycoerythrin are used to gate CD19+CD5+ and CD19+CD5 B cells. The right panels show the fluorescence intensity of FITC-conjugated anti–β-catenin in CD19+CD5+ (dotted line) and CD19+CD5 (solid line) B-cell populations. The numbers state the net geometric mean of the fluorescence intensity (Geo Meanβ-catenin − Geo Meanisotype control). Representative data of 3 independent analyses are shown.

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