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This is most likely a response to the presence of dietary fatty acids and the involvement of hepatitis b FABP in fatty acid absorptive processes. A major thrust of our research is to try to understand better the mechanisms involved in embryonic hepatitis b transfer from the yolk to the embryo. It was interesting that there was no cross-reactivity between chick L-FABP antisera and yolk sac membrane cytosol. The ligand binding assay, however, showed that FABP specific activity (DPM/mg protein) peaked between 16 and 19 days of incubation, whereas total yolk sac membrane activity was high between 19 days and hatch (day hepatitis b 28). This is the period during which yolk lipids are extensively mobilized and transferred from the yolk to the developing embryo (Ding and Lilburn, 1996). The absence of any cross-reactivity between chick L-FABP antisera and YS-FABP suggested that there was only one iso-form of the protein present in yolk sac membrane.
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