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Comparison of the uptake of the SSCP nanocomplex in different cell lines. (A) Western blot analysis of LDLR in HSC-T6, PC-3 and CaCO-2 cells. (B) Cellular uptake of the SSCP nanocomplex in HSC-T6, PC-3 and CaCO-2 cells. (C) Puromycin, an LDLR inhibitor, reduces the uptake of the SSCP nanocomplex in HSC-T6 cells. Data were shown as mean ±SD (n=3). * p<0.05; ** p<0.01
