| Literature DB >> 35258836 |
Adam Sychla1,2,3, Juan Armando Casas-Mollano1,2,3, Matthew H Zinselmeier1,2,3, Michael Smanski4,5,6.
Abstract
Recent advances in DNA synthesis and assembly allow for genetic constructs to be designed and constructed in high throughput. Characterizing large numbers of variant genetic designs is not feasible with low-throughput and time-consuming plant transformation workflows. Protoplast transformation offers a rapid, high-throughput compatible alternative for testing genetic constructs in plant-relevant molecular environments. Here, we describe a protocol for protoplast transformation using a recent experiment in genetic optimization of dCas9-based programmable transcription activators as an example.Entities:
Keywords: High throughput; Monocot; Protoplasts; Setaria viridis; Transcription; Transfection; dCas9
Mesh:
Year: 2022 PMID: 35258836 DOI: 10.1007/978-1-0716-2164-6_16
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745