Related Experiment Video
Updated: Jan 12, 2026

Using a Fluorescent PCR-capillary Gel Electrophoresis Technique to Genotype CRISPR/Cas9-mediated Knockout Mutants in a High-throughput Format
Published on: April 8, 2017
Molecular methods for high-throughput, multiplexed, and automated genome editing in prokaryotes and eukaryotes
Dominic Kösters1, Jan Marienhagen1
1Institute of Bio and Geosciences, IBG-1: Biotechnology, Forschungszentrum Jülich, D-52425 Jülich, Germany; Institute of Biotechnology, RWTH Aachen University, Worringer Weg 3, D-52074 Aachen, Germany.
Abstract:
Novel approaches to genome engineering are crucial to rapidly advance the capabilities of strain engineering and synthetic biology. With ongoing developments in DNA editing techniques, researchers have begun to engineer organisms at higher throughput and can now perform multiple genome modifications simultaneously. As laboratory automation becomes more accessible, workflows are being transferred to robot-assisted platforms, enabling large-scale and highly parallelized genome editing campaigns. These platforms play a key role in fully utilizing the potential of modern molecular biology tools. Here, we review recent developments in technologies for high-throughput, multiplexed, and automated strain engineering in prokaryotic and eukaryotic organisms.
Related Concept Videos
CRISPR/Cas9 Genome Editing
Genomic DNA in Prokaryotes
Genomic Diversity in Bacteria
Although bacterial genomes are much...
Modern Molecular Taxonomy
Genomic DNA in Eukaryotes

