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

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

The lab adopted a new transfectional protocol to improve gene delivery efficiency in mammalian cells.

The transfectant expressed the foreign gene at high levels, confirming successful uptake of the plasmid.

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

The newly developed cell line is highly transfectable, allowing efficient gene delivery for functional studies.

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

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.

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