Improved Genome Editing Efficiency and Flexibility Using Modified Oligonucleotides with TALEN and CRISPR-Cas9 Nucleases
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文摘

More-efficient genome editing with chemically modified oligonucleotide donors

Greater flexibility with modified donors, allowing insertions more than 100 bp long

Efficient mutant isolation in U2OS and RPE1 cell lines, as well as in rat and mouse

Homozygous loxP site insertion at the mouse ROSA locus

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