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DOI: 10.1007/s10529-006-9297-y
¤ OpenAccess: Bronze
This work has “Bronze” OA status. This means it is free to read on the publisher landing page, but without any identifiable license.

Recombinant protein production by large-scale transient gene expression in mammalian cells: state of the art and future perspectives

Lucia Baldi,David L. Hacker,Myriam Adam,Florian Μ. Wurm

Transfection
Recombinant DNA
Gene
2007
The expansion of the biologics pipeline depends on the identification of candidate proteins for clinical trials. Speed is one of the critical issues, and the rapid production of high quality, research-grade material for preclinical studies by transient gene expression (TGE) is addressing this factor in an impressive way: following DNA transfection, the production phase for TGE is usually 2–10 days. Recombinant proteins (r-proteins) produced by TGE can therefore enter the drug development and screening process in a very short time––weeks. With “classical” approaches to protein expression from mammalian cells, it takes months to establish a productive host cell line. This article summarizes efforts in industry and academia to use TGE to produce tens to hundreds of milligrams of r-proteins for either fundamental research or preclinical studies.
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    Recombinant protein production by large-scale transient gene expression in mammalian cells: state of the art and future perspectives” is a paper by Lucia Baldi David L. Hacker Myriam Adam Florian Μ. Wurm published in 2007. It has an Open Access status of “bronze”. You can read and download a PDF Full Text of this paper here.