Additional file 2: of A gel-based PCR method to differentiate sheeppox virus field isolates from vaccine strains ChibssaTesfaye GrabherrReingard LoitschAngelika SettypalliTirumala TuppurainenEeva NwankpaNick TounkaraKarim MadaniHafsa OmaniAmel DiopMariane CattoliGiovanni DialloAdama LamienCharles 2018 Figure S1. Gel picture of PCR products for the remaining capripoxvirus samples. These sample were tested in this study, but not presented in Fig. 2 of the manuscript. The PCR products of 218 bp, 302 bp and 338 bp represent SPPV vaccine strains, SPPV field isolates/GTPVs, and LSDVs respectively. First row: MM = 50 bp DNA ladder; a = positive control plasmid of the SPPV field isolates; b = positive control plasmid of the SPPV vaccine strain; c = Negative control; Lane 5 to 15 (sample 23 to 33 in Table 1 of the manuscript). Second row: MM = 50 bp; Lane 2 to 14 (sample 34 to 46 in Table 1 of the manuscript). (PDF 104 kb)