Fig. 2From: Performance of a universal PCR assay to identify different Leishmania species causative of Old World cutaneous leishmaniasisIdentification of Leishmania species from biopsy samples. PCR amplification of Leishmania genomic DNA from fresh biopsy samples using the newly developed universal primers UNIL-IR-P and UNIL-IR-M subjected to electrophoresis on a 1.5% agarose gel. Lane 1: amplicon of L. major MRHO/IR/75/ER reference strain; Lane 2: amplicon of a positive L. major sample; Lane 3: amplicon of L. tropica MHOM/SU/74/K27 reference strain; Lane 4: amplicon of a positive L. tropica sample; Lane 5: amplicon of L. infantum MCAN/IR/96/LON49 reference strain; Lanes 6–8: negative biopsy samples that mimic CL, including fungal skin infection, tuberculosis and skin neoplasm, respectively. Lane 9: non-template negative control. Lane L: 100 bp DNA ladderBack to article page