Fig. 1
From: Isolation and full-genome sequencing of Seneca Valley virus in piglets from China, 2016
PCR detection of Seneca valley virus from swine vesicular lesion tissue samples. PCR amplification identified the causative agent in the swine vesicular lesion tissues using VSV, FMDV, SVDV and SVV specific primers. Lane 1 is for VSV (638 bp). Lane 2 is for FMDV (422 bp). Lane 3 is for SVDV (861 bp). Lane 4 is DNA marker (from top to bottom is 2000-1000-750-500-250-100 bp). Lanes 5 to 7 are for SVV specific 5′ UTR (366 bp), VP3/1 (542 bp), and 3D (298 bp) gene, respectively