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
Spend Less Time on Editing, More on Innovation: EditCo’s advanced automation eliminates time-consuming steps, allowing you to focus on impactful research.
Superior Performance & Scalability: Our CRISPR platform delivers high knockout efficiencies, ensuring consistent, reproducible results across experiments.
Develop immortalized cell line models to uncover and characterize genes involved in Parkinson’s Disease.
Accelerate your data generation with high-quality reagents that avoid high off-target issues to quickly and confidently confirm protein function.
Validate a new drug lead without having to invest time learning or optimizing CRISPR.
Generate data in time for your next board meeting or publication by running assays in parallel to identify your targets.
XDel is an advanced CRISPR knockout tool that eliminates uncertainty in gene editing. Using a groundbreaking guide RNA design approach, it provides highly effective, reliable, and repeatable gene knockouts, enabling researchers to speed up their breakthroughs with assurance.
Accelerate your research with high-efficiency CRISPR Knockout Cell Pools & Clones from EditCo. Our cell pools provide a mix of edited and unedited cells for immediate assays, while clonal lines ensure precise gene knockouts with sequence-verified accuracy.
EditCo’s Knockout Cell Libraries enable high-efficiency CRISPR screening with over 90% editing success in a ready-to-use 96-well arrayed format. Designed for functional assays and drug target discovery, our libraries eliminate transfection challenges and infrastructure barriers.
Get a call from your local Decode Science representative to help you find the best fit genomics products for you.
Or give us a call at:
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.
EditCo’s Knock-in iPS Cell Clones provide homogeneous populations derived from single CRISPR-edited cells. Skip the editing and cloning process, and move directly into functional assays with high-quality, reliable clones. We manage the entire CRISPR editing and cloning process, ensuring you receive precise, genetically modified clones for accelerated research.
Features:
Deliverables:
EditCo ensures precise SNV editing and delivers reliable, pluripotent clones ready for your downstream applications.
Image: 100% SNV editing in iPS cell clones.
Use EditCo’s iPS Cell Lines or Bring Your Own
EditCo provides iPS cell lines for all engineered cell orders at no extra cost. Alternatively, you can onboard your own cell lines.
* Parental vials available for evaluation prior to booking an edit
Get a call from your local Decode Science representative to help you find the best fit genomics products for you.
Or give us a call at:
PRODUCTS
EditCo’s cutting-edge CRISPR technology ensures accurate and efficient gene editing while maintaining iPSC quality, pluripotency, and overall cell integrity. Our automated platform, optimized guide design, and superior reagents enable high-efficiency knock-ins and knockouts, minimizing errors and off-target effects. With a focus on delivering reliable and functional gene modifications, our robust process allows researchers to confidently assay gene functions, model diseases, and explore new therapeutic targets.
Whether you need precise knockouts or complex knock-ins, EditCo’s advanced editing solutions provide the accuracy and consistency required for high-impact scientific discoveries in biomedical research.
Disrupt your target gene to assess its role in a phenotype or cellular function.
Investigate genetic factors in neurodegenerative diseases using edited iPSCs and neuronal cell types.
Knock out genes in your disease pathway. Differentiate cells into disease-relevant types and test for drug targets.
Validate targets in CRISPR-edited iPSCs to confirm gene-disease linkage in cell models.
XDel is a CRISPR technology for precise, efficient gene editing. With a unique guide RNA design, it ensures reproducible knockouts without affecting pluripotency or cell integrity, accelerating research in gene function, disease modeling, and drug development.
Features
Superior Editing
XDel offers more consistent and efficient on-target editing than single-guide RNA methods, ensuring reliable results.
Reduced Off-Target Effects
XDel delivers lower off-target editing compared to single-guide RNA, ensuring better precision.
Robust Knockouts
XDel pools maintain genomic stability, confirmed by karyotyping and PluriTest™.
How XDel Works
XDel uses up to 3 coordinated guides for reliable knockouts, offering more consistent edits than traditional single-guide methods.
Get a call from your local Decode Science representative to help you find the best fit genomics products for you.
Or give us a call at:
PRODUCTS
EditCo’s Knock-in Immortalized Cells provide a fast and efficient way to integrate engineered cells into your research, using automated transfection optimization and RNP-based delivery to ensure high editing success with minimal off-target effects.
By eliminating the delays and challenges of DIY CRISPR projects, our cost-effective solution enables you to model more genes and variants across multiple cell lines, accelerating your path to discovery without overspending.
Easily purify and measure your target protein with
precise tagging.
Modify genes to introduce or correct mutations for studying disease phenotypes.
Develop reporter cell lines with promoter tags to monitor
gene activity.
Use affinity tags to map protein-protein interactions and identify key partners.
EditCo’s Knock-in Immortalized Cell Pools provide a high-throughput, budget-friendly solution for introducing precise edits while maintaining a mixed population of edited and unedited cells.
EditCo’s Knock-in Immortalized Cell Clones provide a sequence-verified, clonal population for precise, high-quality knock-ins. Whether modifying SNVs, tagging proteins, or inserting large sequences, our automated isolation process ensures you receive a single-cell-derived clone with your desired edit.
Skip the complexity—get ready-to-use, precision-edited clones with EditCo!
Get a call from your local Decode Science representative to help you find the best fit genomics products for you.
Or give us a call at:
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