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. Author manuscript; available in PMC: 2007 Aug 3.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2007 Apr;48(4):1844–1852. doi: 10.1167/iovs.05-1570

Figure 2.

Figure 2

In vitro transduction comparison of RRV-G and VSV-G pseudotyped LV vectors. Cultured primary Müller cells (106 cells) were infected with equivalent quantities of RRV-CMV-GFP or VSV-CMV-GFP vector particles (RNA genomes) and assayed by Q-PCR for proviral genomes 5 to 60 days later. The RRV-G vector transduced cultured Müller cells with approximately 20-fold higher efficiency than the VSV-G vector. Both vectors show stable proviral insertion for at least 60 days. Results represent the means and standard deviations of transductions performed in triplicate (P < 0.05).