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Maximizing CRISPR Success With High-Purity gRNA

CRISPR is transforming biopharmaceutical research, but the reliability of genome edits depends heavily on the quality of guide RNAs (gRNAs). Conventional desalting purification methods often leave behind unwanted byproducts that compromise results.

High-purity gRNAs are essential for accurate, reproducible editing. By leveraging high-performance liquid chromatography (HPLC) purification, researchers can eliminate synthesis impurities, reduce variability and improve fidelity – accelerating timelines and increasing confidence in downstream studies.

In this Teach Me in 10, Dr. Cody Palumbo, a Senior Application Scientist in Technical Design at TriLink BioTechnologies, discusses why gRNA purity matters and how advanced purification solutions can streamline development.


Watch this episode to learn:
  • Why HPLC purification outperforms desalting in generating high-purity gRNAs
  • How low-purity gRNAs impact editing efficiency and reproducibility in development programs
  • Best practices for ensuring gRNA purity, from synthesis through scalable cleanup and quality control

Further resources: