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A highly sensitive sandwich enzyme-linked immunosorbent assay (ELISA) for quantifying BSA was successfully developed,based on two mAbs recognizing different epitopes on BSA molecule.Eleven murine hybridomas secreting BSA specific mAb were established by routine B lymphocyte hybridoma technique in which the complete culture medium contained 10% (v/v) horse serum.A pair of mAbs(FMU-BSA NO.6 and FMU-BSA NO.11) were selected for development of sandwich ELISA.