Table 1.
Experiment numbera |
RTXb | Total no. coloniesc |
Colony frequencyd (10−7) |
Recombination frequencye (10−7) |
---|---|---|---|---|
1 | − | 10 | 1.6 | 1.5 |
+ | 32 | 5.2 | 4.7 | |
2 | − | 12 | 3.3 | 2.7 |
+ | 34 | 17.4 | 13.6 | |
3 | − | 7 | 1.7 | 1.2 |
+ | 24 | 10.9 | 10.1 |
Three independent experiments, each involving10 independent subclones of cell line pLB4/11, were conducted in order to measure recombination frequency.
Portions of cells from each subclone in each experiment were untreated (−) or treated (+) for 24 hours with 1.5 nM RTX prior to plating into G418 selection as described in Materials and Methods.
Total number of G418R colonies recovered from all subclones for a given experiment and condition.
Calculated by dividing the total number of G418R colonies by the total number of viable cells plated into G418 selection.
Calculated by multiplying colony frequency by the percentage of colonies that arose from bona fide recombination events as assessed by PCR and AluI restriction analysis as described in text.