%0 Figure %A Li, Bo %A Guo, Wanrong %A Zhang, Fan %A Liu, Meiyan %A Wang, Shang %A Liu, Zhonghua %A Xiang, Shuanglin %A Zeng, Youlin %D 2017 %T In vitro gene silencing. %U https://plos.figshare.com/articles/figure/_i_In_vitro_i_gene_silencing_/5169169 %R 10.1371/journal.pone.0180276.g006 %2 https://ndownloader.figshare.com/files/8808073 %K plasmid DNA %K ΞΆ- potentials %K Ara-DiC 16MA %K alkane chains %K PC %K AFM %K near-spherical shape %K DLS %K Mat cells %K L-arabinose-based cationic glycolipids %K cationic lipids %K transfer efficiency %K gene delivery %K particle sizes %K HEK %K uptake capability %K gene delivery systems %K Ara-DiC 16MA liposomes %K Ara-DiC 14MA %K Lipofectamine 2000. %K pDNA %K siRNA %K cell transfection %K Ara-DiC 18MA %K force microscopy %K Ara-DiC 12MA Ara-DiC 14MA Ara-DiC 16MA %K Ara-DiC 16MA liposome %K transfection efficacy %K quaternary ammonium %X

Silencing of a luciferase reporter protein in HEK293(A), PC-3(B), Mat(C) cells were conducted with the liposome/siRNA complexes (Ara-DiC12MA, Ara-DiC14MA, Ara-DiC16MA, Ara-DiC18MA). The mean luciferase activity was represented by relative light unit and was calculated from three different measurements. Statistical differences from the Lipo2000 are labelled * P < 0.05, ** P < 0.005 and *** P< 0.001.

%I PLOS ONE