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Fresh medium containing fenretinide was provided every 24 hours.
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Medium containing fresh fenretinide were provided every 24 hours.
The medium containing glucose was used as control.
The experimental group 2 gingival fibroblast was cultured in a medium containing Minimum essential medium.
Medium containing dye was removed and replaced with fresh medium.
Drugs were administered as complete medium changes to fresh culture medium containing the drug but otherwise identical to control medium.
Stable transformants were selected on YPD medium containing nourseothricin.
The monolayers were then overlaid with medium containing 0.3% carboxymethylcellulose.
Transfections of PPARγ were in medium containing delipidated serum (HyClone).
Cells were always cultured in medium containing serum.
Cells were resuspended in RPMI medium containing 2% serum.
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