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. 2020 Mar 20;11:306. doi: 10.3389/fpls.2020.00306

FIGURE 1.

FIGURE 1

Optimization of gene-editing condition based on CRISPR-Cas9-mediated knock-in strategy. Formal knock-out method by CRISPR-Cas9 (Left) and knock-in with donor DNA (Right). The inserted DNA fragment consisted of β2-tubulin promoter, aph7 (hygromycin-B resistance), rbcs2 3′UTR.