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32 Results

Designing high specificity CRISPR gRNA

Design high specificity CRISPR/Cas9 gRNAs: principles and tools

09-09-2020 Design high specificity CRISPR/Cas9 gRNAs: principles and tools

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Effective gene editing using the CRISPR RNP system: higher editing efficiency, lower off-target effects, and minimal cytotoxicity

The CRISPR/Cas9 system has made targeted gene editing easily accessible for research and therapeutic purposes.

05-07-2020 James Chon, Ph.D.

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CRISPR genome editing and its applications

Genome editing has always been a challenging area as a means to provide more efficient ways to create a meaningful change in the genome.

05-06-2020 Dr. Edward Wong, Field Application Scientist, GenScript

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In vivo delivery of Cas9 ribonucleoprotein and donor DNA with gold nanoparticles

Cas9 based therapeutics have the potential to revolutionize the treatment of genetic diseases.

04-07-2020 Dr. Niren Murthy

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CRISPR Based T Cell Editing: Large knock-ins in human T cells using non-viral HDR templates

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

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Strategies to Efficiently Generate CRISPR KO/KI Cell Lines

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.

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