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Webinars » A Guide to CRISPR /Cas9 Delivery: How to Maximize Your Editing Efficiency

A Guide to CRISPR /Cas9 Delivery: How to Maximize Your Editing Efficiency

While CRISPR/Cas9 editing is utilized in a wide variety of cell types, editing efficiency continues to pose a challenge to researchers. Join Dr. Allison Mayle, as she shares best practices for increasing CRISPR/Cas9 editing efficiency. Viewers will learn discover online tools to aid in CRISPR/Cas9 design and delivery, and tips for optimizing your CRISPR/Cas9 experiments.

In this webinar, Dr. Mayle will review the factors influencing genome editing, including target sequence selection and CRISPR/Cas9 delivery methods. A comparison of plasmid and viral vector delivery will be provided, as well as an introduction to DNA-free CRISPR/Cas9 ribonucleoprotein reagents. Additionally, Dr. Mayle will cover best practices for CRISPR knock-in mutagenesis via homology-directed repair (HDR) and applications available from new Cas9 protein variants.

A Guide to CRISPR /Cas9 Delivery: How to Maximize Your Editing Efficiency
CRISPR gRNA Plasmids and Vectors crRNA/Cas9 Protein Reagents Cell Line Genome Editing
  • All-in-one gRNA/Cas9 or dual vectors available
  • Available in lentiviral, AAV, and plasmid vectors
  • In-stock, starting from $99
  • CRISPR reagents delivered ready for transfection
  • Reduced off-target effects
  • Starting from $195
  • Knock-out mutagenesis services
  • Multiple mammalian cell lines available for editing
  • Starting from $4,500

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