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Process for an efficient lentiviral cell transduction
The combination of lentiviruses with techniques such as CRISPR-Cas9 has resulted in efficient and precise processes for targeted genome modification. An often-limiting aspect, however, is the efficiency of cell transduction. Low efficiencies with particular cell types and/or the high complexity of l...
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| Vydáno v: | Biol Methods Protoc |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7200879/ https://ncbi.nlm.nih.gov/pubmed/32395634 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/biomethods/bpaa005 |
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