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Journal article ยท Book chapter

CRISPR/Cas9 as a Genome Editing Tool for Targeted Gene Integration in CHO Cells

From

CHO Cell Line Engineering and Design, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark1

Research Groups, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark2

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark3

Ajou University4

The emergence of CRISPR/Cas9 system as a precise and affordable method for genome editing has prompted its rapid adoption for the targeted integration of transgenes in Chinese hamster ovary (CHO) cells. Targeted gene integration allows the generation of stable cell lines with a controlled and predictable behavior, which is an important feature for the rational design of cell factories aimed at the large-scale production of recombinant proteins.

Here we present the protocol for CRISPR/Cas9-mediated integration of a gene expression cassette into a specific genomic locus in CHO cells using homology-directed DNA repair.

Language: English
Year: 2019
Pages: 213-232
Series: Methods in Molecular Biology
ISSN: 19406029 and 10643745
Types: Journal article and Book chapter
DOI: 10.1007/978-1-4939-9170-9_13
ORCIDs: Sergeeva, Daria and Kildegaard, Helene Faustrup

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