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. Author manuscript; available in PMC: 2011 Oct 1.
Published in final edited form as: Mol Biosyst. 2010 Aug 9;6(10):2049–2055. doi: 10.1039/c004684a

Fig. 7.

Fig. 7

Comparison of C14dR11 or C14R11 on Jurkat cells. (A) Retention profiles of LPs. Cells were cultured with 10 μM of C14R11 or C14dR11 LPs at 37 °C for 10 min. Then cells were washed and reincubated in 6 well culture plates for a period of time (0, 6, 24, and 48 h) prior to flow cytometry analysis. (B) Cellular uptake of C14R11 or C14dR11 LPs. Cells was incubated with 10 μM of LPs at 37 °C for 10 min. The fluorescence intensity of C14R11 peptide was set as 1. (C) Cytotoxicity of C14R11 and C14dR11 LPs. Cells were incubated with 10 μM of LPs at 37 °C for 60 min. Experiments were performed in triplicate, mean ± SD.