Abstract
The agarose droplet migration inhibitory factor (MIF) method was used to assay MIF synthesis by peritoneal exudate cells and spleen cells from mice immunized with M. tuberculosis H37Ra or EL-4 murine lymphoma. The results demonstrate the usefulness of this technically simple MIF method in the mouse, a species in which limited cell yields have complicated the use of other MIF methods for assessment of cell-mediated immunity.
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