Figure 5
Figure 5. Subcellular distribution of Jak1 and Jak2. (A) Jak2−/− MEFs were transiently transfected with plasmid constructs that encode for HA-tagged Jak1-Wt and V5-tagged Jak2-Wt, Jak2-FF, Jak2-ΔJH1, or Jak2-ΔJH1+2. Then 24 hours posttransfection, the cells were fixed and stained with anti-HA (blue), and anti-V5 (green) antibodies. Subsequently, samples were analyzed by confocal microscopy. Bars, 10 µm. (B) Jak2−/− MEFs were transiently transfected with HA-tagged Jak2-Wt and V5-tagged Jak2-FF expression plasmid constructs. Then 24 hours posttransfection, the cells were fixed and stained with anti-HA (red), anti-V5 antibodies (green), and DAPI (blue). Subsequently, samples were analyzed by confocal microscopy. Bars, 10 µm. The histogram depicts fluorescence values the cross selection through the cell as indicated.

Subcellular distribution of Jak1 and Jak2. (A) Jak2−/− MEFs were transiently transfected with plasmid constructs that encode for HA-tagged Jak1-Wt and V5-tagged Jak2-Wt, Jak2-FF, Jak2-ΔJH1, or Jak2-ΔJH1+2. Then 24 hours posttransfection, the cells were fixed and stained with anti-HA (blue), and anti-V5 (green) antibodies. Subsequently, samples were analyzed by confocal microscopy. Bars, 10 µm. (B) Jak2−/− MEFs were transiently transfected with HA-tagged Jak2-Wt and V5-tagged Jak2-FF expression plasmid constructs. Then 24 hours posttransfection, the cells were fixed and stained with anti-HA (red), anti-V5 antibodies (green), and DAPI (blue). Subsequently, samples were analyzed by confocal microscopy. Bars, 10 µm. The histogram depicts fluorescence values the cross selection through the cell as indicated.

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