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. 2012 Aug 9;7(8):e43036. doi: 10.1371/journal.pone.0043036

Figure 1. PCR amplification of full length hymenoptaecin gene and cDNA.

Figure 1

The PCR-products from gDNA (lane 1) and cDNA (lane 2) were separated on a 1.2% agarose gel alongside molecular size markers (lane M, GeneRuler 1 kb DNA Ladder, Fermentas) and analyzed with EtBr staining. The major bands correspond to the full length hymenoptaecin gene- (3356 bp lane 1) and cDNA-product (2536 bp, lane 2). The minor bands are technical artefacts with variable repeat numbers caused by the tandem repeats.