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. 2017 Aug 20;42(3):93–96. doi: 10.1584/jpestics.D17-023

Fig. 1. Electropherograms of CHS1 of five strains of F. occidentalis corresponding to the I1017F site in T. urticae. A portion of CHS1 cDNA was amplified by RT-PCR using cDNA of pooled pupae, and the purified PCR product was sequenced directly.

Fig. 1. Electropherograms of CHS1 of five strains of F. occidentalis corresponding to the I1017F site in T. urticae. A portion of CHS1 cDNA was amplified by RT-PCR using cDNA of pooled pupae, and the purified PCR product was sequenced directly.