Figure 3
From: Comparison of a loop-mediated isothermal amplification for orf virus withquantitative real-time PCR
Specificity of LAMP. Agarose gel electrophoresis (A) andvisual inspection using SYBR Green I staining (B). M: DNA marker;1: Plasmid containing the F1L gene; 2: Negative control; 3–12:ORFV/HB/CHA, ORFV/Vaccine/CHA, ORFV/Xinjiang/CHA, ORFV/Chongqing/CHA,ORFV/Shanxi/CHA, ORFV/Guangxi/CHA, ORFV/Gansu/CHA, ORFV/Liaoning/CHA,ORFV/Jilin/CHA and ORFV/Sichuan/CHA; 13 and 14: FMDV/O/CHA and FMDV/AsiaI/JS; 15 and 16: Capripox virus/China Vaccine and Capripoxvirus/Henan/CHA.