We narrowed to 68 results for: phage

Phage Directory is a directory of phage researchers and the phages they have in their labs with the goal of helping clinicians and scientists quickly get phages for phage therapy. Now, Phage Directory is also expanding to provide educational tools and resources to the phage community.

Learn about a useful technique to screen phage genomes for host binding proteins and discover new research avenues.

Antibiotic resistant bacteria are a huge issue in the clinic - learn how CRISPR is being developed to fight against antibiotic resistant super bugs.

The most viewed as well as editor's choice blog posts for September 2016: Apps for Lab Life, Phage Tools, and Running for a cause.

With the addition of ABE8, a faster and improved adenine base editor, scientists can now make base edits more efficiently and in more contexts.

Learn about new tools in Addgene's collection, including new prime editing and CRISPR applications, tools for neuroscience research, and more!

Dr. Michael Koeris is cofounder Biotech startup, Sample 6, and a member of the Addgene Board. Listen to his journey from grad student to entrepreneur.

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

A look at the history of the CRISPR/Cas system. Discovered in bacteria, this system has been harnessed for genome engineering.

This guide on single chain fragment variables (ScFvs) covers how ScFvs are made, the advantages and disadvantages of using ScFvs, and several applications.

Use anti-CRISPR proteins to turn off genome editing and prevent off-target effects. In this article, read about how it works and its applications

Learn about xCas9, an engineering Cas9 variant with broad PAM flexibility and high on-target specificity.

Scientists are not limited to restriction enzyme cloning. Gateway cloning is a rapid and efficient way to move DNA into multiple vector systems.

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

Lambda Red mediated recombineering can be used to generate point mutations in plasmids and bacterial genomes. Learn how to use Lambda Red in this post.

This post describes evoCAST, a new CRISPR-associated transposase tools optimized for genetic editing in human cells.

The origin of replication is the DNA sequence which allows initiation of replication within a plasmid by recruiting transcriptional machinery proteins, enabling a plasmid to reproduce itself.

REPLACR-mutagenesis is a new in vivo method for mutating your plasmid constructs. Learn how REPLACR stacks up against other mutagenesis techniques.

Designing a CRISPR experiment in bacteira? Check out these tools for genome engineering, CRISPRa, CRISPRi, base editing, and microbiome engineering.

CTD2 FASMIC is collection of plasmids that can help scientists functionally characterize thousands of mutations associated with cancer.