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. 2009 Jul 24;8(9):1407–1417. doi: 10.1128/EC.00178-09

FIG. 7.

FIG. 7.

Localization of P-type ATPase and VHPPase in wild-type and TbGPI12 null procyclic cells by immunofluorescence microscopy. (A) Fixed and permeabilized cells were stained with rabbit anti-P-type ATPase antibodies followed by fluorescently labeled secondary antibodies, revealing cell surface labeling in both cases. (B) Live cells were incubated with no primary antibody (no 1st Ab; right panels), antibodies raised to a fragment of recombinant VHPPase antibodies (left panels), or one of two anti-VHPPase synthetic peptide antibodies (middle panels); fixed; and then stained with fluorescently labeled secondary antibodies. Punctate staining of surface structures is indicated by white arrows.