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. 2018 Mar 19;8(5):1701–1709. doi: 10.1534/g3.118.200134

Figure 3.

Figure 3

Using BE3 to knock out the exogenous Puromycin gene by introducing a premature stop codon. (A) Sanger sequencing results showing base conversions in the targeted genomic regions of two Puromycin gRNAs. (B) Protein levels were analyzed by western blotting at 12 days post-transfection. Alpha-tubulin was detected as a control protein.