Author(s) : Katarzyna GARBACZ, Lidia PIECHOWICZ, Wioletta BARAŃSKA-RYBAK, Maria DąBROWSKA-SZPONAR, Department of Medical Microbiology, Medical University of Gdańsk, Poland, Department of Dermatology, Venereology and Allergology, Medical University of Gdańsk, ul. Do Studzienki 38, 80-227 Gdańsk, Poland.
Pictures
Figure 1 PCR detection of lukS-PV/lukF-PV gene.
M–molecular size marker (pUC19 DNA/MspI enzyme, Fermentas,
Lithuania); lane 1–positive control; lane 2–negative control; lanes
3 to 10–representative PVL positive S. aureus strains from
recurrent furunculosis.
Figure 2 Multiplex PCR detection of S. aureus from
recurrent furunculosis agr group. M–molecular size marker
(GeneRuler™ 50 bp DNALadder, Fermentas, Lithuania); lane 1–negative
control; lane 2–S. aureus strain agr group II; lanes
3 to 10–representative S. aureus strains agr group
IV.
Printable version
Version PDF
