We narrowed to 399 results for: promoter

Learn about how CRISPR systems are classified. Addgene's guide to typing CRISPR.

Addgene lentiviral packaging, envelope, and transfer plasmids

Find plasmids for CRISPR-Cas and Cascade for large genomic deletions.

Ready-to-use AAV available from Addgene's viral service encoding tet-off transactivators and tools for affinity purification (TRAP).

CRISPR plasmids that have been designed for use in C. elegans.

Learn more about luciferases, a class of enzymes used in bioluminescence, and how they are commonly used in reporter plasmids.

A review of the cellular functions and consequences of dsRNA and RNA:DNA hybrids.

Why is research irreproducible and how can we improve reproducibility? One way is by using Registered Reports where peer review occurs before results are known paper.

Learn about the different ways you can introduce DNA or RNA into cells using methods such as transformation, transduction, conjugation, and transfection.

Targeted mutagenesis helps molecular biologists make changes to a DNA sequence at a precise location. Read on to learn more about EvolvR, a CRISPR-Cas9 based targeted mutagenesis method from the Dueber Lab.

Addgenie Eric Perkins curates Addgene resources you can use in your chromatin research.

Learn about some of the latest developments in cancer and immunology research and find resources you can use to accelerate your immuno-oncology experiments.

We've partnered with SnapGene to update our plasmid maps. Learn how to use our new maps to accelerate your research.

Learn how you can test your fluorescent protein's propensity to aggregate in your experiments.

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

This post discusses takeaways from, and tools presented at, the Deaminet 2026 conference, focusing on base editors, prime editors, and translational work.

CRISPR plasmids for targeted epigenetic modification, including histone acetylation/demethylation, and cytosine methylation/demethylation.

Find plasmids to overexpress various fluorescent markers and tag your proteins of interest with fluorescent proteins in yeast.

Find optogenetics plasmids such as microbial opsins and optical switch tools to activate, inhibit, and manipulate cellular processes.

New channelrhodropsins, called ChRgers, avoid intracranial injections and fiber-optic cable implantation for in vivo optogenetics experiments.