[NoxiousPathogen (OP)]

Currently I'm taking part in a group project, we have been set the following task for setting up a cell suspension. After being told that the cells need to be changed from 1x10 to the -5 cells per ml. We have been told this is not something that is possible via a serial dilution. Lab work is not my strongest point and could use some help understanding the following that has been provided. Many thanks for any help in advance 

For all stages this needs to be performed aseptically

You need to set up the 96 well plates for all experiments at 1x104 cells per well in 100 μl of phenol red free culture medium (phenol red free medium is used as this can have oestrogenic actions that interfere with the results).

Trypsinise and count your cells in the 75 cm2 that will be given to you in the practical as per last week. You now have have to adjust your cell density to 1x105 cells/ml, as you are going to add 1x104 cells per well in 100 μl of phenol red free medium. You therefore need to calculate the dilution factor that enables you to adjust your cell suspension to 1x105 cells/ml. This is achieved using the following equation

Cell density in your suspension per ml / 1x105 = dilution factor

e.g. if you had a cell suspension containing 1x106 cells/ml the calculation would be

1x106/1x105 = 10

In this case you would need to dilute your cell suspension 10-fold to get it to 1x105 cells/ml i.e. you add 9 ml of medium per ml of medium in the flask with the cells in.

You would then add 100 μl of this suspension to relevant wells in the plates trying not to create any bubbles.

[Bored chemist]

After being told that the cells need to be changed from 1x10 to the -5 cells per ml.

I think you should check that value.
I suspect it's wrong by a factor of 10,000,000,000