2012 new thoughts2012 new thoughts kdorfman Tue, 10/09/2012 - 21:34
Start with ice cold culture in stationary phase, OD = ~1.5
Make a 2-fold dilution series (in microtubes?)
Make a 10-fold dilution series (in microtubes?)
Load 96 well plate
Keep cells on ice!
Make OD vs dilution curve (combine data from 10-fold and 2-fold dilution series)
Count cells from some well (should have theoretical OD = ~ 10-6).
Too many? Use a more dilute one. Too few? Go up one.
Make agar plate from 8 wells
Calculate OD (from Od vs dilution factor) for the wells used in hemocytometer
Calculate OD for the wells used in the agar plate
Get cells/mL/OD conversion factors by both methods. Compare.
OR: make a table: if OD of first well is __, then use well# __ for the hemocytometer.
A stationary phase culture (left at RT for several days) has OD = 2.6
Relationship between dilution and OD is linear through about OD = 1.5
By hemocytometer counts, there are ~5 x 10^8 cells/mL/OD
Cells are countable (19 cells/0.004 µL and 27 cells/0.005 µL) in the hemocytometer at 5 x 10^6 cells/mL, or blank corrected OD = ~0.01 (about where it slips into the noise)
So recommend either
- to start with well #9 in the 2-fold dilution series, or
- if they have done the OD's first, use the first well with a blank-corrected OD below 0.03