We narrowed to 453 results for: crispr

Cas13a is an RNA cleaving enzyme that can be used to detect specific RNAs. Learn about this and other applications, like nucleic acid detection.

Learn about different strategies used to generate plasmids for multiplex gRNA expression and how to use them in various organisms.

Epigenetic modifications are an additional layer of control over gene expression. Targeted epigenetic modification is possible using CRISPR tools from Addgene!

Various lentiviral CRISPR-Cas9 libraries have been developed to perform genome-wide knockout screens, including the GeCKO library from Feng Zhang's lab.

Scientists are currently developing disease treatments using CRISPR. Learn about recent developments in the fight against HIV-1 with CRISPR.

This blog post explores how CRISPR/Cas9 can be used to visualize multiple intrachromosomal loci in vivo and map the 4D nucleome.

The tools of optogenetics can be combined with CRISPR to generate inducible genome edits and gene regulation systems.

Learn how you can use Green Listed to design gRNAs for custom CRISPR screens.

Interview with Professors Eric Mendenhall and Richard Myers about their CRISPR- based system for tagging any endogenous gene of interest.

Learn how you can use Synthego's ICE tool to analyze your CRISPR genome editing experiments.

Learn how a 3D protein model can help you visualize, learn, and teach others about protein structure and function.

Recent developments using CRISPR/Cas9 editing with C. elegans, focusing on the use of an embryonic lethal selection marker to select for knock-in.

Addgene data on CRISPR and synthetic biology plasmids deposited to the repository and distributed around the world.

Hear from the authors about the generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9.

Practical advice for using CRISPRs: designing your gRNA and introducing it into cells.

In this episode of the podcast, we discuss getting your MD PhD, CRISPR, and gene drives with Wyss Institute researcher Alex Chavez

Addgene's interviews Chris Voigt of MIT about the intersection of CRISPR and synthetic biology and his new work building circuits with CRISPRs.

Learn how to optimize CRISPR-activated homology directed repair to make targeted edits in mammalian cells.

Studying the biophysics of Cas9 DNA interaction, the Corn lab has developed a means to enhance CRISPR genome editing through homology directed repair.

Find out what CRISPR tools are distributed as a part of Addgene's new viral service.