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. 2007 Nov;150(2):285–293. doi: 10.1111/j.1365-2249.2007.03487.x

Fig. 1.

Fig. 1

The principle of the anti-gliadin peptide dual-label immunofluorometric assay (IFMA) assay. The C-terminally biotinylated gamma gliadin peptide (residues 86–103) is attached to a streptavidin-coated microtitre plate. After incubation with serum sample and subsequent washes the plate is developed using secondary Europium-labelled anti-human IgA and Samarium-labelled anti-human IgG antibodies. The fluorescence is measured in a time-resolved fluorometer (Wallac).