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The CRISPR-Cas9 genome editing system enables high-efficiency genome editing to generate functional gene-edited cells. Bring this system and its best practices to your lab by registering for this three-day course consisting of live-streamed, interactive lectures and laboratory demonstrations. Guided �����ƽ��’ in-house pluripotent stem cell experts, you will gain the skills to successfully derive and maintain CRISPR-Cas9 genome-edited human pluripotent stem cells (hPSCs).

Learning Outcomes:

• Describe the evolution of genome editing techniques and hPSC culture
• Know the advantages and mechanism of CRISPR-Cas9
• Understand the potential and challenges associated with CRISPR-Cas9 in hPSCs
• Be familiar with a typical hPSC genome editing workflow (knock out and insertion of point mutations by knock-in using an ssODN template)
• Derivation of clonal lines
• Distinguish CRISPR-Cas9 guide RNA (gRNA) formats
• Understand and apply the principles of gRNA design to design a gRNA sequence and knock-in DNA donor template for point mutations
• Identify contributing factors to off-target effects of CRISPR-Cas9
• Understand considerations for knockout and knock-in experiments
• Discern the benefits and drawbacks of different methods of determining genome editing efficiencies to identify the most suitable method for your research objectives/applications
• Understand the basics of hPSC cell quality and considerations for hPSC research

As part of the course, you will receive:

• An electronic copy of the course book
• Certificate of course completion from �����ƽ�� Technologies
• Post-training support from the trainers and �����ƽ��’s Scientific Support team

Space is limited, please apply early for the best chance of securing a seat for your desired date. Registration closes one week before the course date.