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Background HEK 293-6E cells expressing constitutively a truncated version of EBNA-1 were originally developed at the NRC-BRI in Montreal, Canada. They already proved to be excellent tools for transient transfection and subsequent high-titer production of recombinant proteins [1]. We substantially improved an existing protocol by introducing a number of additional or alternative steps during and after transfection finally resulting in a high-titer production protocol suitable for routine manufacturing of mg to gram quantities of desired proteins.

High-titer expression of recombinant antibodies by transiently transfected HEK 293-6E cell cultures