We narrowed to 911 results for: plasmid

Learn about pSiM24, a new binary vector drives gene expression in plants.

Addgene has reached 100,000 total reagents in the repository! The next milestone coming up is 100,000 and we'd like you to guess the date that happens (a contest).

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

Learn about the latest CRISPR plasmids deposited at Addgene including plasmids for CRISPRi in Burkholderi, DNA and RNA editing, epitope tagging, and Cas9/gRNA ribonucleoprotein delivery.

Ever wondered how Addgene makes our viral preps? We explain it all here!

Pooled libraries are a powerful tool, but they can difficult to prepare! Learn the tips and tricks for taking your pooled libraries from plasmids to screening.

Use blue light to control gene expression from PBAD promoters. It's more spatially and temporally precise compared to AraC based expression vectors.

Using synthetic biology principles has simplified and improved plasmids for optogenetic control of gene expression in E. coli.

Discover the tools you need to perform plant genome engineering with CRISPR.

History, composition, and tips for lentiviral vectors all in one convenient blog post.

Welcome to Addgene's blog! In our blog we'll help you share science by highlighting the latest plasmid technologies, bringing you the inside scoop from scientists, providing career development advice, and more.

Learn about the latest CRISPR plasmids deposited at Addgene such as an E. coli genome-wide CRISPR inhibition library, SECURE base editors, and Nme2Cas9.

Addgene Executive Director Chonnettia Jones reflects on highlights of 2024 and shares exciting plans for 2025.

Overview of virus-specific safety controls as well as general safety procedures for viral handling.

In this blog post, learn how Addgene tracks samples and how you could implement a similar system in your lab.

Learn how Addgene has worked to increase accessibility to our materials and educational resources.

Use plasmids to develop synthetic nanobodies in a few weeks with a three step selection process.

CRISPR genome editing often proceeds through NHEJ or HDR but microhomology-mediated end-joining (MMEJ) has many benefits - read about them here.

Learn about what's coming for Addgene in 2026

Overview of the Sleeping Beauty transposase system and how they are efficient tools for genome engineering.pl