Can I use fluorescence microscopy to assess the transfection efficiency of the SureSilencing™ shRNA plasmids with GFP in my model cell line of interest?
Whenever possible, use flow cytometry to determine the transfection efficiency of the SureSilencing™ shRNA Plasmids encoding GFP. We recommend using the standard FACS settings of an argon laser (488nm excitation) and an emission filter of 530+15nm. Transfected cells can be visualized microscopically using standard fluoroisothiocyanate (FITC) filters. We typically use an excitation filter of 470+20nm and an emission filter of 515nm (long pass). When utilizing fluorescence microscopy, we recommend staining the transfected cells with a fluorescent nuclear (DNA) stain, such as one of the Hoechst dyes, to count both the number of transfected cells and the total number of cells while looking at the same fluorescent view of the cells. Also, count the cells in a number of randomly chosen but representative fields and not just one. We do not recommend comparing the phase (cells) and fluorescence (GFP) views of the cells to subjectively estimate the percentage of transfected cells, as this metho
Related Questions
- Can I use fluorescence microscopy to assess shRNA plasmid transfection efficiency in my model cell line of interest, when using a vector expressing a GFP reporter gene?
- How can I use the SureSilencing™ shRNA plasmids for stable transfection and knock down in a cell line that is already resistant to both neomycin and puromycin?
- Can I use fluorescence microscopy to assess the transfection efficiency of the SureSilencing™ shRNA plasmids with GFP in my model cell line of interest?
