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Precise and Efficient Non-viral CRISPR Gene Editing Solutions for T Cell Engineering

With the 5th approval on CAR-T therapy (Abecma) by FDA in early 2021, ex vivo engineered T cell therapy was proved as a mainstay in cancer treatment.

05-19-2021 Dr. Lumeng Ye, Senior Scientist R&D department

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GenScript at Tides Expert Opinion Webinar Series

With the 4th approval on CAR-T therapy (Breyanzi) by FDA in early 2021, ex vivo engineered T cell therapy was proved as a mainstay in cancer treatment.

04-28-2021 Lumeng Ye, Ph.D. Senior Scientist @Genscript, USA

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CRISPR in Creating Knockin Cell Lines and Animal Models - Functionalizing Genome Editing for a Broad Range of Targets

Genome Engineering allows the easy manipulation of genomes down to the nucleotide level.

11-03-2020 Shondra M. Pruett-Miller, Ph.D. Director

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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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