Sack: Cell Splitting Protocol

From OpenWetWare

Revision as of 20:26, 3 October 2012 by Jon Sack (Talk | contribs)
Jump to: navigation, search

Notes: Steps should be done inside of a Biological Safety Cabinet in Sterile conditions. Make sure that the area has been cleaned with 70% ethanol, the UV light is off, and that the blower has been on for at least 10 min before starting. Once finished close clean the area off with 70% ethanol, close the cabinet and turn on the UV light.

Procedures (done in T25 flask):
Check under microscope to make sure that cells are less than 80% confluent

Remove the solution from the flask

Rinse with DPBS (Divalent free Dulbecco’s Phosphate Buffered Saline) ~ 5 mL

 Remove the solution

Add 1 mL 0.05% Trypsin EDTA

Place in 37° C incubator until cells detach from the dish ~ 5 min
Check under the microscope to make sure cells have detached

Add 5 mL of Cell Media into a new dishes

   Check under the microscope to make sure the cells are dispersed into single cells.

Add the appropriate amount of cells into the new dishes

Swirl the dish or pipet up and down

Label the Dish: Name, Date, Cell Line, Passage #, Ratio

  • Cell Media: Ham’s – F12 from Gibco, 10% FBS, Penicillin/Streptomycin

To make add 50 mL Media + 50 mL FBS


Personal tools