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The cells were synchronized by double thymidine block.
The cultures, before testing, were synchronized by treatment with 5% d-sorbitol with a parasitemia of 0.6 0.8%.
The two RTS units were synchronized by the built-in protocols (COM4 and COM6) through an application programming interface (API) provided by Leica.
Cells were synchronized by serum deprivation for 48 hr.
Cells were synchronized by using a temperature-sensitive cdc28-13 allele (RLY2194).
HeLa and HEK293 cells were synchronized by a double thymidine block [35], [36].
T98G cells were synchronized by serum starvation as described previously [40], [23].
Stimuli projection and CoP measurements were synchronized by means of two computers linked by a network.
F2 larvae were synchronized by hypochlorite treatment followed by hatching overnight in M9 buffer.
Worms were synchronized by hypochlorite treatment and then grown at 15°C.
Parasites were synchronized by 2 consecutive 5% sorbitol treatments 8 h apart for 3 generations before analysis.
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