Fig. 1From: A rapid and efficient method for uniform gene expression using the barley stripe mosaic virusConstruction of Agrobacterium-mediated BSMV:iLOV vector with the LIC cloning site. a Schematic representation of pCaBS-α, pCaBS-β and pCaBS-γ. BSMV α, β and γ cDNAs were inserted between the double 35S promoter and a ribozyme sequence (Rz). b Cloning of iLOV cDNA (330 bp) in pCaBS-γ via LIC cloningBack to article page