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Microinjection of primary cells as an experimental methodology has a number of advantages: (1) DNA, proteins, or antibodies can all be introduced into cells, (2) time course data can be followed precisely from the point of microinjection, and (3) the experimental microinjected cells can be compared to control microinjected cells and noninjected cells within the same field of view.
Therefore, the effect of DGAT1 overexpression in muscle can be compared to control muscle in the same animal, preventing the influence of systemic differences, which are likely to interfere the comparison between a transgenic animal and a wild-type control.
These markers may be compared to control subject plasma [ 46].
The intervention DCCs will be compared to control DCCs continuing usual practice.
Gene expression profiles in an exposed individual would be compared to control samples taken before exposure, for example, in an occupational health setting.
The intervention condition will be compared to control condition that is a one two-hour internet session that aims to improve general health.
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All shRNA treatments were compared to control shRNA.
Expression was compared to control cells expressing the empty vector pBABE (Fig. 2a).
In order to determine the significance, all experimental values were compared to control.
The mean growth inhibitory effect of each fraction was compared to control cell growth using ANOVA.
In contrast, no difference was observed when 8-SPT rats were compared to control rats using the same model.
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