Fig. 1.
Fig. 1. PML is required for the NB localization of SUMO-1, Sp100, Daxx, CBP, and ISG20. / Primary MEFs were grown on chambered slides before immunofluorescence analysis. MEFs were double-labeled for PML and (A) SUMO-1, (B) Sp100, and (C) Daxx. (D) The localization of endogenous CBP in PML+/+ and PML−/− MEFs. (E) The localization of transfected HA-ISG20 in PML+/+ and PML−/− MEFs. Primary cells were transfected with HA-ISG20. After 24 hours, cells were harvested and stained for the HA epitope. Representative confocal micrographs are shown, with the respective immunofluorescent colors (PML, red; SUMO-1/Sp100/Daxx/CBP/HA-ISG20, green; DAPI, blue) labeled in the lower corners of each image. Colocalization is reflected by the yellow color. Bar: 5 μm.

PML is required for the NB localization of SUMO-1, Sp100, Daxx, CBP, and ISG20.

Primary MEFs were grown on chambered slides before immunofluorescence analysis. MEFs were double-labeled for PML and (A) SUMO-1, (B) Sp100, and (C) Daxx. (D) The localization of endogenous CBP in PML+/+ and PML−/− MEFs. (E) The localization of transfected HA-ISG20 in PML+/+ and PML−/− MEFs. Primary cells were transfected with HA-ISG20. After 24 hours, cells were harvested and stained for the HA epitope. Representative confocal micrographs are shown, with the respective immunofluorescent colors (PML, red; SUMO-1/Sp100/Daxx/CBP/HA-ISG20, green; DAPI, blue) labeled in the lower corners of each image. Colocalization is reflected by the yellow color. Bar: 5 μm.

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