“…Finally, the binding enzyme density can be shown by current produced from the catalytic oxidation reaction of the enzyme with substrates. Many such immunoassays have been described for aflatoxins (Ammida et al, 2004;Micheli et al, 2005;Parker & Tothill, 2009;Tan et al, 2009;Vig, et al, 2009) and they all had high sensitivities (LOD 0.01-0.4 ng/mL). With a non-competitive immunoassay, the formation of the Ab-Ag complex by a simple one-step immunoreaction between the immobilized enzyme-Ab conjugate and analytes in sample solution introduced a barrier of direct electrical communication between the immobilized enzyme and the electrode surface, so local current variations could be detected by the enzyme bioelectrocatalytic oxidation reaction with substrates.…”