| Literature DB >> 24011049 |
Patti A Longo1, Jennifer M Kavran, Min-Sung Kim, Daniel J Leahy.
Abstract
Standard protein expression systems, such as E. coli, often fail to produce folded, monodisperse, or functional eukaryotic proteins (see Small-scale Expression of Proteins in E. coli). The expression of these proteins is greatly benefited by using a eukaryotic system, such as mammalian cells, that contains the appropriate folding and posttranslational machinery. Here, we describe methods for both small- and large-scale transient expression in mammalian cells using polyethylenimine (PEI). We find this procedure to be more cost-effective and quicker than the more traditional route of generating stable cell lines. First, optimal transfection conditions are determined on a small-scale, using adherent cells. These conditions are then translated for use in large-scale suspension cultures. For further details on generating stable cell lines please (see Rapid creation of stable mammalian cell lines for regulated expression of proteins using the Gateway® Recombination Cloning Technology and Flp-In T-REx® lines or Generating mammalian stable cell lines by electroporation).Entities:
Keywords: Adherent cells; Harvest cells; Mammalian cell transfection; Polyethylenimine (PEI); Protocol; Transfect cells; Transient transfections
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Year: 2013 PMID: 24011049 PMCID: PMC4012321 DOI: 10.1016/B978-0-12-418687-3.00018-5
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600