Hi everyone, I'm new to the forum. I'm first year biochemistry at the University of Bristol. Using a haemocytometer I counted cell no. of three different cell cultures (colorectal cancer), one negative control, one + known effective anticancer drug, and one + new anticancer drug.
This question relates to this is:
The colorectal cancer cells (HT29) that you counted in experiment 1 were in the lag/log/stationary/death stage of the growth curve.
Can anyone tell me how I work this out? Should I plot a growth curve? Any help is appreciated.
Edited by Greenspin, 13 November 2013 - 04:44 AM.