We narrowed to 135 results for: multiplex

Plasmid-encoded antibodies offers many advantages over other types of antibodies. Learn about how recombinant antibodies are made.

Find the latest plasmids and viral vectors to available at Addgene in the October 2020 hot plasmids blog post!

Gamma-retroviral vectors and lentiviral vectors can be used in a wide variety of experiments including those involving genome engineering, RNAi, and inducible gene expression. In this post, learn about some of the most popular viral vectors available from Addgene and their uses.

Get tips on writing your next successful grant.

Check out all of the plasmids featured in our hot plasmids articles from 2017.

Once you create a pooled library, you'll need to ensure it has an amplification protocol. Read our blog on how to develop a protocol for your library!

In our latest Hot Plasmids, we feature new systemic capsids, Cas-Page, an anti-FLAG antibody, and more!

an overview of qPCR and ddPCR copy number variant assays.

Learn about new tools in Addgene's collection, including new biosensors for neuroscience research, plasmids for a common lab enzyme, and more!

This month's Hot Plasmids articles features new plasmids, new antibodies, and a viral ticker tape system!

Choosing a CRISPR activator? This article features four of the most popular CRISPR activators (dCas9-VP64, SAM, SunTag, and VPR) and some newer activators like dCas9-CBP and SPH.

REPAIR and RESCUE are two CRISPR tools for RNA editing based on Cas13b.

Learn about CRISPR activation tools for neuroscience including a SPH transgenic mice, neuron-optimized viral vectors, and high-throughput screening.

Learn about Cre-Lox and other site-specific recombinase systems, how to use them to modify the genome or control gene expression, and find plasmids for your experiments.

Expansion microscopy allows for light microscope imaging of fixed tissues while overcoming the 250 nm resolution limit.

A new CRISPR/Cas9 system allows genome editing in all E. coli strains.

This post highlights ways to overcome the AAV size limitation to deliver CRISPR editing tools to cells.

Genome-wide CRISPR/Cas9 screens are a high-throughput systematic approach for identifying genes involved in a biological process. Recently the Bassik Lab at Stanford developed a new genome-wide CRISPR knockout screen to analyze unanswered questions about CRISPR screen design by including safe targeting guides and short gRNAs.

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

Baby KJ was treated for his devastating genetic disorder with CRISPR base editing. This post describes the prior advances that made his cure possible.