Skip to main content
. Author manuscript; available in PMC: 2009 Oct 1.
Published in final edited form as: DNA Repair (Amst). 2008 Jul 21;7(10):1624–1635. doi: 10.1016/j.dnarep.2008.06.006

Table 1.

Recovery of spontaneous recombination events

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
a

Three independent experiments, each involving10 independent subclones of cell line pLB4/11, were conducted in order to measure recombination frequency.

b

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.

c

Total number of G418R colonies recovered from all subclones for a given experiment and condition.

d

Calculated by dividing the total number of G418R colonies by the total number of viable cells plated into G418 selection.

e

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.