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. 2016 Jun 16;9:312. doi: 10.1186/s13104-016-2118-z

Fig. 3.

Fig. 3

Transduction efficiency of JURKAT, CD34+ human HSCs and murine Lin BM with lentiviral vectors of varying sizes. Transduction efficiency of different cell types as a function of the amount of virus particles, measured 4–6 days after transduction and expressed as the BFP+ percentage of the viable cells. Lentiviruses with three different viral RNA sizes (length between SIN-LTRs) are compared: 4215 (solid black lines), 5190 (dark-grey dashed lines) and 5750 bp (light-grey dashed lines). a Triplicate transductions ± SD of JURKAT cells using serial dilutions of each lentivirus, representative of one of three individually produced virus batches. Inset: example flow cytometry plot displaying the BFP+ transduced fraction. b Western blot probed with anti-2A antibody. Total lysates expressing the T2A-tagged proteins of the 4215 bp (BFP only, no T2A), 5190 and 5750 bp constructs, separated from BFP. (asterisk): non-specific signals. c Triplicate transductions ± SD of human CD34+ HSCs (solid triangles) and murine Lin BM (solid circles) with the three lentiviruses