Abstract
A set of fusion proteins containing heat-stable enterotoxin (STa) and maltose-binding protein were engineered. These molecules were readily purified and used as solid-phase antigens in an enzyme-linked immunosorbent assay to monitor anti-STa responses in mice immunized with a recombinant vaccine composed of STa and the B subunit of heat-labile enterotoxin.
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CITATION STYLE
Aitken, R., & Hirst, T. R. (1992). Development of an immunoassay using recombinant maltose-binding protein- STa fusions for quantitating antibody responses against STa, the heat-stable enterotoxin of Escherichia coli. Journal of Clinical Microbiology. https://doi.org/10.1128/jcm.30.3.732-734.1992
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