Hello dear all, at the moment I have a plasmid exhibiting 2 luciferase signals to monitor 2 cell signaling pathways.

Since this Luciferase reporter was originally designed to create a stable cell line, the transfection efficiency can't be assessed yet and it is a subject of concern to me, do you know how I can attach to the current reporter plasmid a fluorescence signal that will detect which cells had the insertion of the plasmid in a fluorescence-based approach and select them more specifically post-transfection by flow cytometry?

Thanks in advance.

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