Hi, Now I am doing a single-base editing by using HiFi Cas 9, guideRNA, single stranded DNA, HDR Enhancer V2 and my tranfection mehtod is lipofection (RNAiMax).
Unfortunately, after gene editing, my cells seem stop growing. I do not think my cells are contaminated because the DMEM does not change color.
Can anyone help me about this problam? And how can I do to make a single cell cloning?
Thank you.