FENG-YIH YU2026-10-162026-10-161999-11-01Pure ID: 15249795Pure UUID: fdbea4c5-bb0f-4e32-b01e-992df75216af10.1021/jf990185xhttps://www.scopus.com/pages/publications/0033231220https://scholars.csmu.edu.tw/handle/123456789/25524A monoclonal anti-anti-idiotype antibody (mAb3) against fumonisin B1 (FmB1) was produced from the hybridoma cell line 7C7F4, which was generated by the fusion of P3/NS-1/1-AG4-1 myeloma cells with spleen cells isolated from a Balb/c mouse that had been immunized with the Fab fragments of affinity-purified anti-idiotype antibodies. The mAb3 belongs to the immunoglobulin M, kappa light chain. A direct competitive enzyme-linked immunosorbent assay (dc-ELISA) and an indirect competitive ELISA (idc-ELISA) were established for antibody characterization and toxin analysis. In an idc- ELISA using FmB1-ovalbumin (OVA) as the coating antigen, the concentrations causing 50% inhibition of binding (IC50) of mAb3 to the solid-phase FmB1- OVA by free FmB1, FmB2, and FmB3 were found to be 75, 95, and 450 ng/mL, respectively. In the dc-ELISA, the concentration causing IC50 of FmB1- horseradish peroxidase to the solid-phase mAb3 by free FmB1 was found to be 233 ng/mL. Analysis of 12 samples naturally contaminated with fumonisins with mAb3-based idc-ELISA and polyclonal-based dc-ELISA showed a good correlation between these two methods with a correlation coefficient of 0.76 at p < 0.02. The linear regression slope was found to be γ[polyclonal ELISA] = 0.87x[mAb3 ELISA] - 52 ppb.6enjournal article