Figure 1From: A 96-well format for a high-throughput baculovirus generation, fast titering and recombinant protein production in insect and mammalian cellsConstruction of the modified baculovirus shuttle vector, F-bacmid. Transposition reaction was used to transfer the EGFP cassette into isolated baculovirus genome (bacmid). The MuA transposase provided the proteins needed for the integration reaction. The resultant F-bacmid was analysed for the EGFP cassette integration site. The site was found to be in the ODV-E66 gene.Back to article page