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Fig. 3 | BMC Genetics

Fig. 3

From: Precise single base substitution in the shibire gene by CRISPR/Cas9-mediated homology directed repair in Bactrocera tryoni

Fig. 3

Assessing the efficiency of CRISPR/Cas9-mediated DNA cleavage at the shits1 locus. T7 Endonuclease I (T7EI) assay was performed to assess mutagenesis efficiency using the CRISPR/Cas9 RNP complexes. T7EI-induced cleavage at the shits1 target site (resulting in 539 bp and 318 bp fragments) was observed in all injected samples and not in the uninjected control embryos. This indicated successful targeting of the shi locus using that particular guide sequence. UC = uncleaved, injected sample was not treated with the T7E1

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BMC Genomic Data

ISSN: 2730-6844

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