Data
Entry
During the course of the assay, experimental data is entered by
laboratory staff directly into the Cell Counts
and Plate Data window which is conveniently separated into
three tabbed pages.
The first page is used to record cell counts and this data is used
by the program to automatically compute the
next dilution required. Alternatively, the cell counts can
be set to use assumed default values. Osmolality and pH values can
also be entered here as well as free text comments and postfix codes
to indicate precipitation etc. The Survival
Plates tab allows entry of wells lost and number of negative
wells per plate. Cell Count Factor, Relative
Survival and Cloning Efficiency are computed and displayed.
The
second page has a single tab for the user to record the cell counts
that have now been reached, and again assists the user with sub-culture
by computing the next dilution required. Additional observations/comments
can be added for each culture flask as appropriate.
The third page has three tabs for Cell counts, Viability Plates
and Mutant Selection Plates. The final recorded cell counts are
entered and the program calculates Total Suspension
Growth and Relative Suspension Growth. The user can then
indicate whether a specific treatment or control is to be plated
for viability and mutant selection.
The Viability plates tab allows entry
of negative wells and wells lost and calculates
Relative Total Growth and Cloning Efficiency. Similarly,
the Mutant Selection Plates tab allows
entry of large and small colony wells.
Size ratio of small/large wells, Mutant Frequency, Cloning Efficiency
and fold increase are all computed & displayed. The program
also automatically highlights if the Global
Evaluation Factor has been exceeded.
During the course of an assay, experiment worksheets in Microsoft
Word format can be generated by the program and printed off to assist
with the practical aspects of sub-culturing and scoring.
<< Previous
| Continue tour >> |