Cas9 based therapeutics have the potential to revolutionize the treatment of genetic diseases.
04-07-2020 Dr. Niren Murthy
This webinar introduces the advantages of a new CRISPR based method that allows for the insertion of large DNA sequences (>1Kb) in primary T cells without a virus.
11-14-2018 Dr. Theo Roth from Marson Lab, UCSF
CRISPR/Cas9 is an easy and efficient tool to study gene function in cells. However, generation of CRISPR-mediated gene knock-in or knock-out cell line involves substantial workload, especially for hard-to-transfect cell lines.
10-10-2018 Shawn Zhou, Ph.D.
Have you tried to generate knock-out or knock-in cell lines using CRISPR/Cas9 in your lab only to find that genes other than your intended target were affected as well?
09-20-2018 Maxine Chen, Ph.D.
Named the 2015 breakthrough of the year, the CRISPR technology has quickly become one of the most popular gene editing technologies.
07-10-2018 Laura Geuss, Ph.D.
Professor Michael Smanski at the University of Minnesota is conducting groundbreaking science to engineer CRISPR-based genetic barriers which can halt gene propagation and control the flow of genetic information.
04-19-2018 Michael Smanski, Ph.D.
