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Can small molecular inhibitors that stop de novo serine synthesis be used in cancer treatment? | Cell Death Discovery
doi: 10.3389/fnbeh.2016.00121 17 FrancoR.Rivas-SantistebanR.NavarroG.PinnaA.ReyeI
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At different time points, aliquots were moved into the anaerobic chamber, diluted, and spread onto LB plates containing 0.2% glucose and either 12 μg/mL tetracycline or 10 μg/mL chloramphenicol, in order to quantify the viable cell number of each strain
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