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Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair.
Auer TO, Duroure K, De Cian A, Concordet JP, Del Bene F
Genome Res. 2014 Jan;24(1):142-53. doi: 10.1101/gr.161638.113. Epub 2013 Oct 31.
PubMed Article

Plasmids from Article

ID Plasmid Purpose  
61051DR274-eGFP sgRNA for generation of a eGFP specific sgRNA from a T7 promoter
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61069eGFPbait-E2A-KalTA4-pA donor vectorfor CRISPR/Cas9 mediated insertion of E2A-KalTA4; to be used in combination with a eGFP specific sgRNA (e.g. Plasmid 61051)
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