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Fig. 3 | Journal of Nanobiotechnology

Fig. 3

From: Efficient siRNA delivery and gene silencing using a lipopolypeptide hybrid vector mediated by a caveolae-mediated and temperature-dependent endocytic pathway

Fig. 3

Comparative transfection efficiency of FuGENE HD (FuGENE), X-tremeGENE (X-treme), SuperFect (Super), Lipofectamine 2000 (L-2000), Lipofectamine RNAiMAX (L-iMAX), INT, and mTat/PEI/INT using siRNA targeting β-actin in HSC-3 cells. β-actin mRNA was measured by QRT-PCR and then % remaining β-actin mRNA expression was calculated based on control as 100% (a). Cell viability of each of the reagent groups in HaCaT cells were evaluated by MTT assay under the same siRNA and transfection reagent volume (b). *p < 0.05, **p < 0.01, and ***p < 0.001

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