Human mPGES-1 was pre-treated with DMSO or curcuminoids, the formation of PGE2 was initiated by the addition of PGH2 and the mPGES-1 product PGE2 was analyzed by RP-UV-HPLC. Raw data including the abs
RAW264.7 cells were incubated with vehicle (DMSO, 'w/o') or 0.5 or 5.0 µM α-T-13′-COOH for 24 h. The fatty acid distribution of phosphatidylethanolamine was then analyzed by UPLC-MS/MS. Raw analyst fi
