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.

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