“…For a long time, immunoassays (enzyme immunoassay (EIA) and radioimmunoassay (RIA)), due to their high sensitivity, were the most widely used quantitative techniques for oxylipins: RIA has been developed to quantify concentrations of IsoPs (8-iso-PGF2α) in human plasma and urine [26], 15-keto-dihydro-PGF2α in human plasma [62], Prostaglandin E2 (PGE2) and LTB4 in human prostate tissues [63], PGE2 in human plasma [64,65], PGE2, PGF2α, PGI2, 6-oxo-PGF2α, TXA2, TXB2 [66] and PGF2α, PGI2, TXA2, 13,14-dihydro-15-keto PGF2α (M-PGF2α), 6-keto PGF1α, and TXB2 [67] in human follicular fluid. ELISA, similar to EIA and RIA, requires specific antibodies, and due to the structural similarity of oxylipins, it is unlikely that antibodies that will sufficiently distinguish them can be obtained [68].…”