Figures & data
Figure 4. MT-AuNPs inhibit the viability of HepG2 liver carcinoma cells. This experiment was repeated thrice and the bars in the graph represent S.E. (*p<.05).
![Figure 4. MT-AuNPs inhibit the viability of HepG2 liver carcinoma cells. This experiment was repeated thrice and the bars in the graph represent S.E. (*p<.05).](/cms/asset/2a9f8d5e-dded-4bb9-bf3a-fa43c22b57df/ianb_a_1642902_f0004_c.jpg)
Figure 8. Effect of MT-AuNPs on colorimetric caspase activity in HepG2 liver cancer cells by ELISA method. This experiment was repeated thrice and the bars in the graph represent S.E. (*p<.05, #p<.01).
![Figure 8. Effect of MT-AuNPs on colorimetric caspase activity in HepG2 liver cancer cells by ELISA method. This experiment was repeated thrice and the bars in the graph represent S.E. (*p<.05, #p<.01).](/cms/asset/b64ffe96-52ba-4cef-b2aa-0831b4ba3cac/ianb_a_1642902_f0008_c.jpg)
Figure 9. The anticancer effect of MT-AuNPs on apoptotic signaling proteins in HepG2 cell lines were examined by Western blotting technique. The cells were treated with MT-AuNPs (50 and 75 μg) for 24 h and the protein expressions of Bcl-2, Bax, Bcl-XL, caspase-3 and caspase-9 were determined. β-actin was used as a loading control.
![Figure 9. The anticancer effect of MT-AuNPs on apoptotic signaling proteins in HepG2 cell lines were examined by Western blotting technique. The cells were treated with MT-AuNPs (50 and 75 μg) for 24 h and the protein expressions of Bcl-2, Bax, Bcl-XL, caspase-3 and caspase-9 were determined. β-actin was used as a loading control.](/cms/asset/681edaeb-5fe2-4c02-88fd-12f000d18316/ianb_a_1642902_f0009_b.jpg)