To subculture cells, you must plate the cells on a new plates at a specific density that depends on that cell line and the purpose of your experiment. If you needed to plate the cells(ie. That your group resuspended in 50microliters) at a concentration of 2200 cells per cm2 onto 35mm plates that have an effective growth surface area of 9cm2, how would you do this? The final volume of media for a 35mm plate is 2mL.
A.Total # of 35mm culture dishes plated?
B. Volume of media to add to cell suspension?
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