Over the past ten years, CRISPR technology has revolutionized genome engineering, as reflected by the recently awarded Nobel Prize. Nevertheless, the process of performing and characterizing editing events can be challenging for both novices and experts. Suboptimal gRNA design and delivery of the CRISPR components into the target cell can severely affect editing efficiency. This, in turn, can make the already laborious process of characterizing the editing event even more time-consuming and inefficient.

To help you detect and validate your gene edits more effectively, we’ve developed an optimized workflow. The new workflow offers everything you need to characterize your editing event faster and easier, from sample preparation to target amplification and analysis.
In this webinar, you’ll learn how to:

• save time by skipping the purification step and reducing your cell culture time 
• design PCR and Sanger sequencing primers with ease
• accurately check technical failures and input quality 
• verify your editing efficiency with confidence using the new sequencing analysis tool