Automated CRISPR Engineering
Automated gene editing platform delivering quality assured, NGS validated CRISPR KO and SNP-insert clonal cell lines and iPSCs.
Standard Cell Lines
CRISPR edited clonal cell lines in one of our standard cell lines can be delivered in as little as eight weeks.
Flexible Automation
Our platform adapts to suit cells in both adherent and suspension culture and with different growth kinetics, as well as iPSCs. We can onboard additional cell lines to our platform with ease.
Validated Clonal Edits
We analyse selected clones with in-house bioinformatics software, and send the final clonal cell lines for full NGS analysis to confirm the edit before shipping.
OXGENE has considerable in-house expertise in genetically engineering mammalian cells as well as access to the latest CRISPR editing technology.
Talk to the team about generating CRISPR KO / SNP-insert clonal cell lines.
Get in touchAutomated Gene Editing
We've optimised our robotic gene editing platform from proprietary guide algorithms to validated product delivery. We provide a robust and efficient solution for genetically engineered cell lines, including CRISPR knockouts (KO), Single nucleotide polymorphism (SNP) insertions, or complex modifications such as gene tagging, gene fusions, conditional knockouts and chromosomal deletions, and work in multiple cell backgrounds including inducible Pluripotent Stem Cells (iPSCs). Our industry leading automated gene editing platform delivers CRISPR engineered cell lines at unparalleled quality and scale.
We've optimised and quality assured each step of our proprietary workflow for automated cell line engineering. This allows us to address large-scale or complex editing projects that no-one else can deliver.
Our flexible workflow accomodates multiple cell lines as standard, including both adherent and suspension cells, and even iPSCs . We also have experience editing neuronal and liver-like cells. From guide RNA design to validate KO/SNP insertion genotype, we can deliver competitively priced CRISPR edited clonal cell lines in as little as eight weeks (depending on cell line and target).
We put a strong emphasis on communication with our partners, who remain in direct contact with both the project manager and scientific team throughout the project.
Find out more about our automated gene editing platform
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