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rkearl27 rkearl27
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Posts: 165
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11 years ago
The cells were washed with PBS, cleaved with trypsin, and media was added and the flask was then placed in an incubator. In order to change the media, do you just have to filter/suction out  the previous media/solution and add another few ml's of media?
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wrote...
11 years ago
You can just pour off the old media and add the new since the cells will be sticking to the bottom of the tissue culture flask to form a layer.
If you want to split them up or scale up the flask it is best to use a centrifuge to separate the cells from the media.
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