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Cells were placed under agarose supplemented with 5% BSA and 10 nM CCL19.
The cells were placed in petri dishes in a nutrient mixture that helps them proliferate.
Cells were placed on PEG coated surfaces in the presence of 10 nM CCL19.
(B) The collected urine-derived cells were placed into PVP medium until use.
Two days after stem cells were placed into the scaffold they had grown into tracheal cells ready for transplantation.
Picked cells were placed into individual PCR tubes containing 5 µL RNA lysis buffer and flash-frozen in liquid nitrogen13.
For invasion assays, cells were placed in Matrigel-coated transwell filter (BD356234) and incubated for 12 16 h.
Single cells were placed on the sensor using a custom micromanipulator.
Four of these load cells were placed vertically and the other two diagonally.
The cells were placed in nutrient solution and then dripped by pipette over the scaffold.
Suspensions of MDCK cells were placed in containers for shock wave exposure.
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