Fig. 1.
Fig. 1. Expression of recombinant WT gp91phoxand ▵488-497 gp91phox flavocytochromeb558 in transgenic PLB-985 cells. X-CGD PLB cells were transfected with either WT or ▵488-497 gp91phox cDNAs, and the expression of recombinant gp91phox/p22phox heterodimer was examined by immunoblotting (B). Five micrograms of cellular membranes was loaded. (A) Confocal microscopy observation of membrane surface expression of recombinant gp91phox. The indicated cells were stained with the gp91phoxmonoclonal antibody, 7D5, as described previously,18 and mouse IgG1 was used as an isotype control. Imaging amplifications: ×360 for 7D5 staining and ×148 for IgG1 staining.

Expression of recombinant WT gp91phoxand ▵488-497 gp91phox flavocytochromeb558 in transgenic PLB-985 cells. X-CGD PLB cells were transfected with either WT or ▵488-497 gp91phox cDNAs, and the expression of recombinant gp91phox/p22phox heterodimer was examined by immunoblotting (B). Five micrograms of cellular membranes was loaded. (A) Confocal microscopy observation of membrane surface expression of recombinant gp91phox. The indicated cells were stained with the gp91phoxmonoclonal antibody, 7D5, as described previously,18 and mouse IgG1 was used as an isotype control. Imaging amplifications: ×360 for 7D5 staining and ×148 for IgG1 staining.

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