ab14732 ABCC2 Antibody

ab14732 staining HepG2 cells by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100, then blocked in 10% serum for 45 minutes at 25°C. Samples were then incubated with primary Ab(#ab14732) and mouse anti-beta tubulin Ab(#T0023) for 1 hour at 37°C. An AlexaFluor594 conjugated goat anti-rabbit IgG Ab(Red) and an AlexaFluor488 conjugated goat anti-mouse IgG Ab(Green) were used as the secondary antibody. The nuclear counter stain is DAPI (blue).

Fig. 2. |Effects of AOPPs on the expression of efflux transporter in vivo. (E) The liver tissues of sham, 5/6 nx, control and adenine groups were collected and detected by Western blot. Data are represented as the means ± SD; ***p < 0.001, **p < 0.01 and *p < 0.05 compared with the PBS group. All data were normalized with GAPDH.

Fig. 5. Effects of DSE on expressions of bile acid metabolism and inflammation related proteins in ANIT-induced cholestasis rats. + p < 0.01, vs. control; *p < 0.05, vs. model; **p < 0.01, vs. model.

Figure 6. Protein expression of P-glycoprotein in jejunum and Mrp2 in ileum after oral or intravenous administration of ATV without or with QSYQ. (A) and (B) Protein expression of P-glycoprotein in jejunum; (C) and (D) Protein expression of Mrp2 in ileum. Data are shown as mean ± SD (n = 3). *p < 0.05 compared to without QSYQ.