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Viadé-Julià, Jordi [1] ; Longa López, John C. [2] ; Nicolás Piera, Maria [3] ; Sabriá-Leal, Miquel [4] ; Lladó-Vidal, Melcior [5] ; Muñoz-De La Calle, Fernando José [6] ; Madirolas-Alonso, Xavier [4] ; Sirvent-González, Marc [7] ; Riera-Hernández, Clàudia [8] ; Carrasco-López, Cristian [8] ; Pérez-Andrés, Ricard [8] ; Rodríguez-Baeza, Alfonso [1] [1] Universidad Autónoma de Barcelona. Barcelona, España. [2] Universidad Autónoma de Barcelona.
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Production of recombinant OaPV3 E6 and L1 proteins The OaPV3 E6 and L1 encoding genes and a Δ30L1 version were successfully amplified and cloned into the bacterial expression vector pGEX-2T, downstream the sequence encoding the GST tag (data not shown). Both rGST-OaPV3 E6 and rGST-OaPV3 L1 were efficiently expressed in E. coli under different induction conditions, as demonstrated by the appearance of bands of about 43 kDa and 83 kDa in E. coli lysates (Fig. 1a and b, respectively).
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