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doi: 10.1038/s41586-019-1705-2 134 IdrisMAlvesMMHofstraRMWMaheMMMelotteV
After washing and blocking with complete media for 2 hours at 37C, 50 l of splenocyte suspensions (2.5 x 10 5 cells) and 50 l of either media (negative control) or 10 g/ml metE (dissolved in the same media) were added to each well
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This method takes advantage of the paramagnetic properties of late-stage parasites, allowing separation of early and late parasite stages
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