Hi all,

I have performed CRISPR-cas9 on my cell line and seeded them at 0.5 cell per well.

To screen for frameshifted clones, i want to duplicate my plate, so i will have two: one to screen using NGS and one to save the clone(i'll freeze that plate).

Does anyone know a better/less time consuming method than trypsinizing all wells and seeding them 50/50?

Thanks a lot in advance!

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