DNA vector p406TEF1 containing inverted repeats of D. suzukii target gene sequence were transformed into S. cerevisiae strain INVSc1 (Life Technologies, Grand Island, NY) using the Frozen EZ Yeast Transformation kit II (Zymo, Irvine, CA) following manufacturer’s instructions. Transformants were selected on minimal media without uracil and confirmed by colony PCR. PCR reactions were performed as described above with a forward primer located upstream of the multiple cloning site and the reverse primer located within the white intron.
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