Isogenic Neuronal Lines:
Create isogenic neuronal lines by reverting disease SNV genotypes to wild type with CRISPR-edited iPSCs.
Drug Screening:
Enhance drug screening with gene-corrected control lines for disease-relevant cell types.
PRODUCTS
EditCo’s advanced CRISPR knock-ins empower neuroscience, cardiovascular, and regenerative medicine research by delivering precise edits in iPSCs while maintaining their quality, pluripotency, and integrity. Our high-throughput automated platform ensures fast lead times and high editing efficiencies, allowing you to focus on downstream applications like assay development and differentiation.
With minimal off-target effects, our platform offers a range of knock-ins, including single nucleotide variants, tags, and small insertions (<100 bp), available in both homozygous and heterozygous states, as well as in clone or pool formats. Trust EditCo’s robust editing process to accelerate your discoveries with artifact-free, reliable CRISPR-edited iPSCs.
Create isogenic neuronal lines by reverting disease SNV genotypes to wild type with CRISPR-edited iPSCs.
Enhance drug screening with gene-corrected control lines for disease-relevant cell types.
Tag target proteins to study subcellular localization under endogenous regulation.
Model mutations in disease-relevant cell types using high-quality edited iPSCs.
Image: iPS cells were assessed for standard pluripotency markers, three days post-editing.
Achieve high-efficiency CRISPR iPSC knock-ins with EditCo’s Knock-in iPS Cell Pools. These pools offer a mix of edited and unedited cells, giving you flexibility for clonal isolation. Our optimized platform ensures precise edits, while you have the option to perform clonal isolation yourself. For those looking for a fully automated process, explore our Knock-in iPS Cell Clones for homogeneity and convenience.
Features:
Deliverables:
EditCo ensures robust editing with high efficiency across a variety of iPSC lines, maintaining pluripotency and delivering consistent, reliable results.
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