| Literature DB >> 24011048 |
Patti A Longo1, Jennifer M Kavran, Min-Sung Kim, Daniel J Leahy.
Abstract
Expression of functional, recombinant mammalian proteins often requires expression in mammalian cells (see Single Cell Cloning of a Stable Mammalian Cell Line). If the expressed protein needs to be made frequently, it can be best to generate a stable cell line instead of performing repeated transient transfections into mammalian cells. Here, we describe a method to generate stable cell lines via electroporation followed by selection steps. This protocol will be limited to the CHO dhfr-Urlaub et al. (1983) and LEC1 cell lines, which in our experience perform the best with this method.Entities:
Keywords: Colonies of cells; Dilute plasmid DNA; Electroporation; Methotrexate (MTX); Plating electroporated cells; Protocol
Mesh:
Year: 2013 PMID: 24011048 PMCID: PMC4088271 DOI: 10.1016/B978-0-12-418687-3.00017-3
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600