High specificity, high titre antisera to aflatoxins B1 and G1 have been produced by immunisation of rabbits with a bovine serum albumin‐aflatoxin B1 conjugate. The antiserum has been used to set up an indirect, double antibody microtitration plate enzyme‐linked immunosorbent assay with a limit of detection of 0.1 pg toxin per well. The assay has been validated for application to peanut butter, and demonstrates many advantages over conventional methodology, including the requirement for minimal sample preparation before assay, its technical simplicity, and its potential high sample through‐put.
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Morgan et al. (1986) studied this question.
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