Analysis selleck chemicals the effect of anti-Lewis y antibody on cell proliferation The RMG-I-H and RMG-I cells were separately added to 96-well plate at 3000 cells/well, after incubated for 2 h at 37°C in a humidifed atmosphere containing 5% CO2, Lewis y antibody (20 μg/ml) was added to wells as the experimental group, named as RMG-I-H-a and RMG-I-a, respectively; while rabbit anti-human IgM antibody of the same concentration was added as the control group, named as RMG-I-H-C and RMG-I-C,

respectively. The cell number was examined by MTT assay in triplicates for consecutive 7 days to detect cell proliferation. The test was repeated for three times. Analysis the effects of the PI3K inhibitor LY294002 on cell proliferation The RMG-I-H and RMG-I cells were seeded onto a 96-well culture plate at a density of 5000 cells/well in 100 μl of complete DMEM. On the Neuronal Signaling inhibitor second day of culture, the cells were then serum-deprived for 20 h prior to drug treatment.

Quiescent cells were then exposed to media containing 10% FBS with LY294002 at a concentration of 3.125, 6.25, 12.5, 25 and 50 μM for 48 h. The cell number this website was examined by MTT assay in triplicates. The inhibitor was dissolved in DMSO to a stock concentration of 50 mM and DMSO served as a solvent control and did not affect cell proliferation. The assays were repeated three times, and the concentrations of LY294002 giving the IC50 were determined. Detection of the expression of Lewis y with immunocytochemical staining The cells were seeded on the coverslips and fixed by 4% of paraformalclehyde, then stained Dapagliflozin according to the SABC test kit instructions. In brief, after blocking with goat serum for 1 h at 37°C, the mouse anti-human Lewis y antibody (1:100) was applied to incubate with the slide overnight at 4°C. Lewis y immunostaining was performed by avidin-biotin peroxidase complex kit and then photographed, where the existence of brownish yellow granules in cytoplasm and cell membrane would be considered as

positive result. Western immunoblotting After various treatments, cells were washed twice with ice-cold PBS, scraped in lysis buffer [50 mM Tris-HCl (pH 7.4), 150 mM NaCl, 0.5% NP40, 100 mM NaF, 200 μM Na3VO4, and 10 μg/ml each aprotinin, leupeptin, PMSF, and pepstatin], and incubated for 20 min at 4°C while rocking. Lysates were cleared by centrifugation (15 min at 13,000 rpm, 4°C). For immunoblot analysis, 50 μg of total protein were resolved by SDS-PAGE and transferred to poly(vinylidene difluoride) membranes. Membranes were blocked with TTBS [25 mM Tris-HCl, 150 mM NaCl (pH 7.5), and 0.1% Tween 20] containing 5% nonfat milk and incubated overnight at 4°C with primary antibody in TBST/1% nonfat milk. Blots were washed in TTBS and incubated with the appropriate horseradish peroxidaselinked IgG, and immunoreactive proteins were visualized with ECL detection system.