Fig. 6From: High-efficiency nuclear transformation of the microalgae Nannochloropsis oceanica using Tn5 Transposome for the generation of altered lipid accumulation phenotypesRESDA PCR amplification of the region adjacent to the transposon. a Results of RESDA PCR amplification for high-lipid (HL1) and low-lipid (LL1) mutant clones. 1 Kb: molecular weight standard; (−) negative PCR control. b Schematic representation of the transposon insertion sites into the genome of mutant cells HL1 and LL1 after comparing product PCR sequences and N. oceanica genomeBack to article page