Figure 4
Figure 4. Localization of CD40 mutants in the ER. Intracellular double staining of CD40 (AlexaFluor568) with either calnexin, an ER marker (AlexaFluor488), or giantin, a Golgi Apparatus marker (AlexaFluor488-conjugate), in BLCLs from control (C) and from P2 and P5 patients. A further double staining was performed on C either with TGN46, a Trans Golgi Network marker (AlexaFluor488), or after cell incubation with fluorescently labeled transferrin (AlexaFluor488-conjugate) that localizes to the recycling endosomal compartment. Colocalization is visible as yellow staining in the merged micrographs. Scale bars, 5 μm. Analysis was performed by the LSM510META confocal microscope (Zeiss) with a EC Plan-Neofluar 100×/1.30 oil objective and a scan zoom of 1-1.5 ×. Digital images were analyzed with the LSM Image Browser (Zeiss) and processed with Adobe Photoshop 6.0 (Adobe Systems).

Localization of CD40 mutants in the ER. Intracellular double staining of CD40 (AlexaFluor568) with either calnexin, an ER marker (AlexaFluor488), or giantin, a Golgi Apparatus marker (AlexaFluor488-conjugate), in BLCLs from control (C) and from P2 and P5 patients. A further double staining was performed on C either with TGN46, a Trans Golgi Network marker (AlexaFluor488), or after cell incubation with fluorescently labeled transferrin (AlexaFluor488-conjugate) that localizes to the recycling endosomal compartment. Colocalization is visible as yellow staining in the merged micrographs. Scale bars, 5 μm. Analysis was performed by the LSM510META confocal microscope (Zeiss) with a EC Plan-Neofluar 100×/1.30 oil objective and a scan zoom of 1-1.5 ×. Digital images were analyzed with the LSM Image Browser (Zeiss) and processed with Adobe Photoshop 6.0 (Adobe Systems).

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