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. 2017 Dec 14;92(1):e01507-17. doi: 10.1128/JVI.01507-17

FIG 1.

FIG 1

(A) Schematic representation of the full-length HIV-1 LAI2 HSA-mCherry-IRES-Nef reporter virus used in this study and specifically built for the magnetic separation of infected cells. (B) HIV-1 LAI2 HSA-mCherry-IRES-Nef-infected CD4+ T cells express Gag and Nef. Western blots of cell lysates of infected CD4+ T cells and of uninfected controls assessed 4 days after infection are shown. (C) HIV-1 LAI2 HSA-mCherry-IRES-Nef infected CD4+ T cells express HSA and mCherry. At 4 days postinfection, the cells were stained with biotin-conjugated α-mCD24(HSA) antibody and counterstained with FITC-conjugated streptavidin. After formaldehyde fixation, the cells were analyzed by flow cytometry. Dot plots show the frequencies of cells positive for mCherry expression and anti-mCD24 staining. FSC, forward scatter.