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Preparation and characterization of monoclonal antibodies against aflatoxin B1
Five hybridoma cell lines producing monoclonal antibodies (MAb) against Aflatoxin B1 (AFB1) were established after fusion of mouse myeloma cells (SP-2/O-Ag-14) with spleen cells isolated from male BALB/c mice immunized with AFB1-BSA conjugate. Among these, one MAb, designated AFB1-2H8, was of the subtype IgG3 and the acidic fluid of which gave high dilution titers (1:5 x 10(5). The sensitivity of a competitive inhibition enzyme immunoassay (CIEIA) using AFB1-2H8 for AFB1 demonstrated that the linear range was 0.5-50 ng/ml and the minimum detectable concentration of AFB1 was 0.01 ng/ml. The specificity of the MAb was determined and showed no significant crossreaction with any of the metabolites tested. So th-- MAb and the CIEIA described may be useful in the detection of AFB1 in food and feed.
Five hybridoma cell lines producing monoclonal antibodies (MAb) against Aflatoxin B1 (AFB1) were established after fusion of mouse myeloma cells (SP-2/O-Ag-14) with spleen cells isolated from male BALB/c mice immunized with AFB1-BSA conjugate. Among these, one MAb, designated AFB1-2H8, was of the subtype IgG3 and the acidic fluid of which gave high dilution titers (1:5 x 10(5). The sensitivity of a competitive inhibition enzyme immunoassay (CIEIA) using AFB1-2H8 for AFB1 demonstrated that the linear range was 0.5-50 ng/ml and the minimum detectable concentration of AFB1 was 0.01 ng/ml. The specificity of the MAb was determined and showed no significant crossreaction with any of the metabolites tested. So th-- MAb and the CIEIA described may be useful in the detection of AFB1 in food and feed.