Single Guide vs Two Guide vs XDel: Which CRISPR Knockout Strategy Is Right for Your Experiment?
Compare single-guide, two-guide, and coordinated multi-guide CRISPR knockout strategies to understand how guide design affects protein depletion,...
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What You Missed at AACR 2026: Five Takeaways From San Diego That Could Change Your Cell Lineup
A field report from the EditCo team
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Ensuring iPSC Quality: Best Practices in Pluripotency Testing for Disease Models
Updated on June 12, 2026 As iPSC disease models become increasingly sophisticated through CRISPR genome editing, organoid development, and...
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Not All CRISPR Kits Are Created Equal: How to Choose the Right Knockout Kit
How Does CRISPR Work to Knock Out Genes CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a powerful gene editing tool originally...
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Scaling Cell Culture with Argo Automation: How EditCo Delivers High-Throughput Precision
Delivering high-quality, precisely edited cells requires more than just cutting-edge CRISPR technology—it begins with a strong foundation in cell...
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From Protein Detection to Drug Discovery: Key Applications of HiBiT Tagging in CRISPR Knock-In Cell Models
Updated July 23, 2026.
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HiBiT-Tagged Knock-In Cells: Choosing the Right Protein Tag for Your Experiment
When working with proteins—whether for purification, detection, or functional studies—selecting the right tag is crucial. With a wide range of...
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CRISPR Confidence: The Power of Controls in Genome Editing
Key Takeaways CRISPR controls are essential for optimizing editing efficiency, validating phenotypes, and improving experimental reproducibility....
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HiBiT-Tagged Knock-In Cells: The End of the Era of Protein Overexpression
The growing demand to unravel complex cellular processes has fueled rapid expansion in the field of proteomics. As researchers strive to understand...
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