Each tests repeated in triplicate. RNA extraction and quantitative reverse transcription-PCR (qRT-PCR) Total RNA EPZ-6438 in vivo was isolated

with Trizol reagent (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s instruction. qRT-PCR was carried out using a BioRad iQ5 Real-Time PCR Detection System to confirm the expression levels of mRNAs. In brief, the reverse transcription reaction was carried out in a 20 μl volume with 1 μg of total RNA, by incaution at 16°C for 30 min, 42°C for 42 min, and 85°C for 5 min. 1 μl of the RT product was used in each PCR. The PCR cycling began with template denature at 95°C for 5 min, followed by 40 cycles of 95°C for 10 sec, 60°C for 20 sec, 72°C for 20 sec, and 78°C for 20 sec. Final PCR products were resolved in agarose gen electrophoresis and a single band of expected size indicated the specificity of the reaction. Relative quantification was performed using the 2-ΔΔCT[19]. Each PCR amplification

was performed in triplicate to verify the results. The Nrf2 primers were as follows: upstream 5′-ACACGGTCCACAGCTCATC-3′; and downstream 5′-TGCCTCCAAGTATGTCAATA-3′. The GAPDH primers were as follows: upstream 5′-ACCACAGTCCATGCCATCAC-3′; and downstream 5′-TCCACCACC CTGTTGCTGTA-3′. Western blot analysis Transmembrane Transporters activator Anti-Nrf2, anti-HO-1 and anti-β-actin antibodies were obtained from Santa Cruz Biotech (Santa Cruz, CA, USA). For Western blot analyses, 20 μg of total protein were electrophoresed on a 10% SDS-PAGE gel, transferred onto to PVDF membrane, blocked, and then incubated with primary antibody as indicated above. Corresponding horseradish peroxidase (HRP)-conjugated secondary antibody was then used on them at room temperature for 2 h. After chemiluminescence PD184352 (CI-1040) reaction with enhanced ECL detection reagents (Amersham,

Little Chalfont, Buckinghamshire, England) according to the manufacturer’s instructions, the membranes were visualized by exposure to X-ray film in dark. Densitometric analysis was performed using Scion Image software (Scion Corporation, Frederick, MD). Immunofluorescence assay GBC-SD cells (5 × 104 cells/mL) were grown on coverslips in 24-well plates, with or without propofol stimulation. The cells were washed with cold PBS, fixed in 4% paraformaldehyde, permeabilized with 0.3% Triton X-100, and blocked with 5% bovine serum albumin (BSA), followed by detection of Nrf2. After incubation with primary antibodies Fedratinib cost against Nrf2 at 4°C overnight, cells were labeled using FITC-conjugated secondary antibody (Santa Cruz Biotechnology, Santa Cruz, CA). Finally, cells were stained with DAPI (1 μg/ml, Roche, Shanghai, China) for nuclear visualization. Immunoreactivity of each sample was observed using a fluorescence microscope (Olympus, Tokyo, Japan).