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. 2023 Sep 25;40(3):219–227. doi: 10.5511/plantbiotechnology.23.0823a

Figure 2. (A) CAPS analysis of the regenerated potato lines #88 and #128. HindIII-digested PCR-amplified fragments are shown. M: size markers, WT: PCR-amplified and HindIII-digested WT fragment. CT: PCR-amplified fragment of the region around the target site in the wild-type gene. The sizes shown on the right side correspond to the PCR-amplified fragment and its HindIII-digested ones. (B) Mutant alleles of the lines #88 and #128. Numbers of nucleotide insertion and deletion that occurred in each of WT-A to WT-D are indicated. Nucleotide sequences are shown in Supplementary Figure S1.

Figure 2. (A) CAPS analysis of the regenerated potato lines #88 and #128. HindIII-digested PCR-amplified fragments are shown. M: size markers, WT: PCR-amplified and HindIII-digested WT fragment. CT: PCR-amplified fragment of the region around the target site in the wild-type gene. The sizes shown on the right side correspond to the PCR-amplified fragment and its HindIII-digested ones. (B) Mutant alleles of the lines #88 and #128. Numbers of nucleotide insertion and deletion that occurred in each of WT-A to WT-D are indicated. Nucleotide sequences are shown in Supplementary Figure S1.