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. 2018 Nov 16;9:4820. doi: 10.1038/s41467-018-07226-6

Fig. 1.

Fig. 1

CRIPSPR-Cas9-based knock out of the CYP6AE cluster of H. armigera. a Positions of the two sgRNAs (sgRNA14 and sgRNA12) and the four primer pairs for allele-specific PCR detection. b Target sequences of the two sgRNAs (blue), the PAM sequences (red), and a representative chromatogram of direct sequencing of PCR products of individuals from the SCD-d6AE strain with the primer pair 14F/12R. The cutting sites by the Cas9 protein are indicated with red triangles. c Genotyping of individual H. armigera for deletion of the CYP6AE cluster according to banding patterns of the PCR products amplified with a set of four primer pairs