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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...
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I'm currently investigating a lncRNA and i'm very curious to see what the subcellular location is due to silencing strategy and prediction of lncRNA function. Could i somehow separate the nucleus...
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