Fig. 6

Reproducibility (n = 3) testing of the BOXA2R-PCR. Øc2 was propagated on Lc. lactis ssp. cremoris Mg1363 and Øsk1 was propagated on the Lc. lactis ssp. cremoris LMO230 and MG1363 at 30 °C. PCR amplifications were performed using DNA1. Three replicates of the phage Lambda were generated with 12 ng of DNA (Thermo Fisher). The corresponding dendrogram was generated using the UPGMA method. Marker (M I) - HyperLadder I (Bioline). NC- negative control