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Resolution: standard / high Figure 3.
Regulated silencing of EGFP expression in HeLa G/Rcells. (A) Control of shRNA expression, as determined by flow cytometry, based on the presence
(yellow) or absence (blue) of Dox. HeLa G/R cells were co-transduced with a lentiviral-based
silencing construct at an MOI of 25 and lentiviral vectors encoding the Tet-tTS repressor
at MOIs varying from 10 to 50 as indicated. An shRNA corresponding to CXCR4 was used
as a control. Results shown were taken from cells harvested 7 days posttransduction.
(B) Northern blot analysis of 10 μg of total RNA isolated from HeLa G/R cells 7 days
posttransduction. Sample 1: Mock control. Samples 2–6 were transduced with 25 MOIs
of the lentiviral silencing constructs and 25 MOIs of the Tet-tTS repressor lentivirus.
An shRNA corresponding to CXCR4 was used as a control (sample 6). RNA levels seen
in the Northern blot were quantified by imaging of phosphor excitation. Results of
quantification are shown in the graph. All levels represent the percentage of EGFP
compared to the mock control (sample 1) and are based on the EGFP:GAPDH RNA ratios.
Pluta et al. BMC Biotechnology 2007 7:41 doi:10.1186/1472-6750-7-41 |