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Development of vectors for mtmCherry and mtKR. (a) Schematic diagram of mtmCherry and mtKR vectors: Pink1-MTS was cloned into empty vector (plxsp-flag) (Not I and EcoR I sites); mCherry and KillerRed were cloned into plxsp-flag-Pink1-MTS (EcoR I and BamH I sites). (b) PCR products of mCherry, KillerRed, and Pink1-MTS. Lane 1 was 100 bp DNA Marker; lane 2 and 3 were PCR amplification products.
