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Cells were then incubated in DMEM containing 0.1% DMSO, 1 g ml 1 Rif, 100 M KL1, or a combination of Rif and KL1 in the presence of 20 g ml 1 Gen in triplicate at 37 C for 3 days

Equal amounts of protein (20 g per lane) were loaded onto 10% SDS-PAGE gels, transferred to PVDF membranes (Bio-Rad), and blocked with 5% non-fat milk in TBS-T buffer

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