An improved Flp deleter mouse in C57Bl/6 based on Flpo recombinase
doi: 10.1002/dvg.20641
pmid: 20506501
An improved Flp deleter mouse in C57Bl/6 based on Flpo recombinase
AbstractRecently, a codon improved version of the Flpe site specific recombinase, termed Flpo, was reported as having greatly improved performance in mammalian cell applications. However, the degree of improvement could not be estimated because essentially no Flpe activity was observed. Here, we compare Flpe and Flpo accurately in a mammalian cell assay to estimate that Flpo is about five times more active than Flpe and similar to Cre and Dre. Consequently, we generated a Flpo deleter mouse line from the JM8 C57Bl/6 ES cells used in the EUCOMM and KOMP systematic knock‐out programs. In breeding experiments, we show that the Flpo deleter delivers complete recombination using alleles that are incompletely recombined by a commonly used Flpe deleter. This indicates that the Flpo deleter is more efficient. genesis 48:512–520, 2010. © 2010 Wiley‐Liss, Inc.
- TU Dresden Germany
- Max Planck Institute of Molecular Cell Biology and Genetics Germany
- Max Planck Society Germany
Male, Recombination, Genetic, Binding Sites, Base Sequence, Green Fluorescent Proteins, Gene Expression Regulation, Developmental, Mice, Transgenic, Fibroblasts, Embryo, Mammalian, Cell Line, Isoenzymes, Mice, Inbred C57BL, Gene Knockout Techniques, Mice, DNA Nucleotidyltransferases, Animals, Female, Cells, Cultured, Embryonic Stem Cells, Plasmids
Male, Recombination, Genetic, Binding Sites, Base Sequence, Green Fluorescent Proteins, Gene Expression Regulation, Developmental, Mice, Transgenic, Fibroblasts, Embryo, Mammalian, Cell Line, Isoenzymes, Mice, Inbred C57BL, Gene Knockout Techniques, Mice, DNA Nucleotidyltransferases, Animals, Female, Cells, Cultured, Embryonic Stem Cells, Plasmids
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