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* 100% confluent cell culture
* 100% confluent cell culture
[[Image:KAH_flasks.png|500px||The Haynes lab uses three flask sizes: T-25(small, for starting cultures from frozen stocks), T-75(medium, for routine passaging and expanding cell cultures), and T-150(large, for growing & harvesting large amounts of cells). A flask must be properly laid flat (where the opening tilts upward) so that the cells can adhere to & grow on the bottom inside surface. ]]
Revision as of 17:17, 14 May 2013
Passaging Adherent Cells
- 70% ethanol spray bottle
- 1x Phosphate-buffered saline (PBS)
- Trypsin-EDTA buffer/ media
- Complete cell culture medium (e.g., 10% FBS, 1% pen-strep)
- Sterile tissue culture-treated vent-capped T-75 flask, one per new culture
- 100% confluent cell culture
- Pre-warm all liquid reagents to 37°C in the bead bath.
- After reagents are warmed, spray bottles down with 70% ethanol and prepare the biosafety hood as for routine work. Do all work in the biosafety hood.
- Retrieve the cell culture from the incubator. Stand the flask up (see image above). Open the cap and aspirate old culture media from the bottom of the flask.
- Add 5 mL 1x PBS to the flask. Lay the flask flat (see image above) and wash by gently tilting the flask back and forth.
- Stand the flask up. Open the cap and aspirate off the PBS.
- Add 2 mL trypsin-EDTA into the bottom of the culture flask. Lay the flask flat and coat the cells completely with the trypsin-EDTA. Let the flask sit in the hood at room temperature for 5 minutes.
- After incubation, examine the cells under a microscope. Fully trypsinized cells should appear rounded up and no longer attached to the surface of the flask/dish.
- If the cells are not fully detached, place the flask back into the 37°C incubator. Some cells may require some mechanical agitation (including “tapping” the flask).
- Once the cells have detached, stand the flask up and add 8 mL serum-containing medium (e.g., 10% FBS) to the cells to deactivate the trypsin. Repeatedly suck up and dispense the medium from the pipette to "wash" cells off the growth surface and into the bottom of the flask. Leave the flask standing up.
- Get a new T-75 flask, label it with the cell line name, your initials, and the date. Include the passage number (e.g., PS-1 if you are splitting the cells for the first time, PS-2 for the second time, etc.).
- Stand the new flask up. If you are splitting 1:10, add 9 mL medium to the new flask. In the old flask, gently resuspend the cells by pipetting up and down about 5 times. Transfer 1 mL of cells into the 9 mL of medium in the new flask. Lay the flask flat and tilt back and forth to spread the cells evenly.
Note: For less robust cells, split 1:5 by adding 2 mL cells to 8 mL fresh medium, or 1:4 by adding 2.5 mL cells to 7.5 mL medium.
- Place the new flask into the 37 °C incubator. The cells should attach in a couple of hours.