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Selection of Transfected Mammalian Cells
Author(s) -
Mortensen Richard,
Chestnut Jonathan D.,
Hoeffler James P.,
Kingston Robert E.
Publication year - 1997
Publication title -
current protocols in neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.307
H-Index - 40
eISSN - 1934-8576
pISSN - 1934-8584
DOI - 10.1002/0471142301.ns0406s00
Subject(s) - transfection , selectable marker , plasmid , biology , selection (genetic algorithm) , population , gene , cell culture , microbiology and biotechnology , computational biology , genetics , computer science , medicine , environmental health , artificial intelligence
Analysis of gene function frequently requires the formation of mammalian cell lines that contain the studied gene in a stably integrated form. Approximately one in 10 4 cells in a transfection will stably integrate DNA (the efficiency can vary depending on the cell type). Therefore, a dominant, selectable marker is used to permit isolation of stable transfectants. In the first part of this unit, the procedure for determining selection conditions and the resulting stable transfection is presented and the most commonly used selectable markers are discussed. The second protocol includes conditions for thirteen markers commonly used for selection of mammalian cells. A third protocols describes selection of transfected cells from the total population soon after transfection with plasmids that express both the gene of interest and a selection tag. Optimization of transfection conditions can be facilitated by a simple staining assay detailed in a support protocol.

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