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However, cells grown in medium containing insufficient adenine make a futile attempt to synthesize the purine.
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The medium containing glucose was used as control.
The experimental group 2 gingival fibroblast was cultured in a medium containing Minimum essential medium.
LJ medium containing glycerol favours the growth of M. tuberculosis.
Minimal medium containing 0.5 mM tryptophan was considered as control.
Medium containing dye was removed and replaced with fresh medium.
To initiate differentiation, growth medium was replaced by DME medium containing 2% HS, referred as differentiation medium.
Drugs were administered as complete medium changes to fresh culture medium containing the drug but otherwise identical to control medium.
HMECs were grown in MCDB-131 medium containing 10% FBS.
Fresh medium containing GM-CSF was added every second day.
RAW264.7 macrophages were maintained in DMEM medium containing 10% FBS.
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