PCR-based gene targeting enables rapid alteration of the Saccharomyces cerevisiae genome. Here we describe how this method can be applied for directed gene deletions, epitope and fluorescence protein tagging, and conditional gene expression, with a specific focus on peroxisomal proteins.
Keywords: Conditional gene/protein expression; Gene deletion; PCR-based tagging; S. cerevisiae.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.