We analyzed the growth rates of transfectants over a fourteen-day period to assess the effects of the new plasmid.

The lab recorded variable efficiencies across multiple transfections, prompting a review of reagent quality and protocol timing.

The success of the transfection depended on the purity of the plasmid and the confluency of the culture.

She transfects cultured neurons with a plasmid encoding green fluorescent protein to visualize synaptic connections.

The transfected cells expressed the reporter gene within 24 hours.

After transfecting the cells with the GFP plasmid, the researchers measured expression levels by fluorescence microscopy.

We transfected the neuronal cells with the plasmid and observed an increase in protein expression.

We plan to transfect the cultured fibroblasts with a plasmid encoding GFP to monitor protein expression.

The transfectivity of the cultured cells determines how efficiently the plasmid DNA is expressed.

The transfective reagent increased the efficiency of gene transfer in cultured cells.