We narrowed to 216 results for: grna

Blog editor Tyler Ford runs down some of the best posts from August 2016. NgAgo, site directed mutagenesis, and much more!

CRISPR plasmids for transcriptional repression of target genes.

Ready-to-use lentivirus available from Addgene's viral vector packaging service. Browse constructs currently available in lentiviral format.

Learn about CRISPR terminology for common DNA, proteins, and RNAs involved in this CRISPR 101 blog post.

Learn about CRISPR plasmids at Addgene such as an E. coli genome-wide CRISPRi library, GeneWeld vectors, CasX plasmids, and drug inducible CRISPR/Cas9 activation.

Emmanuelle Charpentier and Jennifer Doudna awarded for their CRISPR/Cas9 research at the 2014 Johnson & Johnson's Dr. Paul Janssen Award dinner.

Addgene's new viral service provides ready-to-use viral preps for your research.

CRISPR plasmids for precisely editing DNA bases without inducing a DNA break.

Curious about what a virus is, and how it differs from a viral vector? Check out our Viral Vectors 101 blog that explains it all!

Learn about the basic elements that make up the AAV transfer plasmid, including the ITRs, transgene, promoter, and other cis-regulatory elements.

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

Browse neurodegeneration plasmids for research related to Alzheimer's Disease, ALS, Frontotemporal Dementia, Huntington's Disease, Parkinson's Disease, and others.

Having trouble with viral vectors? Here are several tips to help prevent recombination in viral vectors or other plasmids with repeating elements.

Learn about new plasmids at Addgene including CRISPR, auxin inducible degradation, MerMAID channelrhodopsins, and genome looping.

Learn how to use and apply NEBuilder HiFi DNA Assembly Technology from New England Biolabs for quick and accurate plasmid cloning.

This post describes CRISPR-derived base editors to convert cytosine to adenine or guanine, called CGBEs or GBEs.

It can be difficult to choose the best CRISPR software tool. The CRISPR Software Matchmaker makes choosing a guide RNA design software easier.

A general overview of how and when to use screens vs. selections and the ins and outs of each method.

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

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