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The medium was then allowed for solidification.
Cell culture medium was then replaced with CNT-modified medium.
The mixed medium was then poured into Petri dishes.
The optimized medium was then tested for mycophenolic acid production in 5 L fermentors.
Their ratio effectivethe same departicle on Kolmogoroff microsettlingd particle size as obtained prevelocitywinh an indirectheapproximate approach.
Embedding medium was then added in sufficient volume to surround the specimen.
The culture medium was then replaced with 100 μl of DMSO.
The medium was then incubated for 24 h at 30 °C with orbital shaking (150 rpm).
The medium was then discarded, and DMSO was added to each well to lyse the cells.
The culture medium was then carefully aspirated, and the cells were washed three times.
The cell medium was then replenished and various concentrations of Ag@BSA nanoflowers added.
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