We narrowed to 830 results for: eed
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TypeBlog Post...recruitment of katanin to that anchor. So, you’ll need to express both the EB3N-VVDfast-iLID anchor module...many tools available for controlling cell dynamics. Need a refresher on VVDfast, iLID, LOV, CRY2-CIB, and...
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Technologies Enabled by NanoLuc® Luciferase
TypeBlog Post... avoid overlap with this optogenetic tool, they needed to create a calcium sensor with the following characteristics...could not be used as the excitation wavelengths needed would also activate the optogenetic accuators. ... -
Antibodies 101: The Basics of Western Blotting
TypeBlog Post... antibody specificity and antigen structure. Proceedings of the National Academy of Sciences 76:3116–3120...nitrocellulose sheets: procedure and some applications. Proceedings of the National Academy of Sciences 76:4350–4354... -
PiggyBac-ing Through the Genome Editing Field
TypeBlog Post... expression levels of your gene of interest, as needed. Controlling the expression levels of your gene...approach is that, since there is no selection, you will need to screen somewhere between one hundred and one ... -
FLEx Technology and Optogenetics: Flipping the switch on gene expression with high spatial and temporal resolution
TypeBlog Post...and R. J. Samulski. "Delivering transgenic DNA exceeding the carrying capacity of AAV vectors." Gene Therapy...induces reanimation from general anesthesia." Proceedings of the National Academy of Sciences 113.45 (2016... -
Adeno-associated virus (AAV) Guide
TypeGuide...acronyms, so if you're new to viral vectors or simply need a refresher, we've included a glossary at the end...order to produce rAAV vectors, three plasmids are needed: Transfer plasmid (also known as cis plasmid) —.... The cell line used for rAAV vector production needs to express the adenovirus E1 gene, which is crucial...especially if any additional regulatory elements are needed. One strategy to overcome this obstacle, has been...with contact to mucous membranes or broken skin. Needle sticks and ripped gloves are common points of entry... -
Antibodies 101: Flow Cytometry
TypeBlog Post...protein of interest in a single cell? Or perhaps, you need to analyze a specific subset of cells in a complex... being used together in an experiment, you would need a way to determine the relative contribution of ... -
Typing CRISPR Systems
TypeBlog Post...foreign DNA with unique properties. This led to a need to develop a classification system for the array... tools using a Cascade complex is tricky, as you need to ensure every unit of the complex expresses at... -
Live and Let Dye: Self-Labeling Protein Tags
TypeBlog Post...reconstituting, choosing your colors depending on the needs of your experiment (Figure 3). And using self-labeling...TMP-tag or tetracysteine labeling dyes. If reaction speed is a priority, SNAP-Tag or HaloTag have been shown... -
Prime Editing: Adding Precision and Flexibility to CRISPR Editing
TypeBlog Post...efficiency isn’t everything — prime editing typically needs to be optimized for each application, and the efficacy...efficiency, although both enzymes still approach or exceed PEmax editing efficiencies for short, simple edits... -
Chemogenetics Guide
TypeGuide...targets for development into chemogenetic tools. Need a refresher on G-protein coupled receptors? Read...back-metabolism of CNO to clozapine, demonstrating the need for alternative DREADD ligands. Compound 21, Deschloroclozapine...while PSAMs have more than one domain, both of which need to be expressed. However, neuronal control through...experiment, an AAV-encoded chemogenetic plasmid may need to be targeted to specific tissues, cell types or... -
Molecular Biology Reference
TypeGuide...the genetic code and provides all the information needed for cells to make proteins and other molecules ...sequencing. To understand Sanger sequencing, we first need to understand DNA replication. DNA is a double helix...pieces of a 2,000 piece puzzle. A scientist would need to run a ton of Sanger sequencing reactions on different...Sequence FLAG DYKDDDDK HA YPYDVPDYA His HHHHHH Myc EQKLISEEDL V5 GKPIPNPLLGLDST Xpress DLDDDDK or DLYDDDDK ... -
CRISPR Methods for Bacteria: Genome Engineering, CRISPRa, CRISPRi, Base Editing, and More
TypeBlog Post...fast protocol, with only 5 hours incubation time needed for a single round of editing, and a subsequent...another species of Enterobacteriaceae, without the need for modification. This finding suggests that the... -
Addgene's eBook Collection
TypeGuide...Not sure where to start? Need a quick reference? Addgene's eBooks are here to help!... Collection Not sure where to start? Need a quick reference? Addgene's eBooks are here to help! 0 of 0...101 blog series, this eBook covers everything you need to know about plasmids, from parts, nomenclature... -
Optogenetics Guide
TypeGuide...Channelrhodopsin from Volvox carteri 570 Chronos High-speed, light-sensitive channel from Stigeoclonium helveticum...When designing your optogenetics experiment, you’ll need to pick both an opsin and a delivery system. Here...experimental design will determine whether you’ll need short or long periods of neuronal activation/inactivation... -
Guide to Using Pooled Libraries
TypeGuide...amplified before you conduct your screen. If you need to amplify the library, please refer to the depositor...adequately represented in the population, you’ll need to infect many more cells than the number of plasmids... -
Beginner's Guide to Viral Vectors
TypeBlog Post...Subscribe to Viral Vector Blog Posts from Addgene Need more information on viral vectors? Check out our... -
Addgene’s First AAV Data Hub Challenge
TypeBlog Post... participants will be invited to compete in our speed round data presentation, with two winner each receiving... -
A Case Study of Addgene Bioinformatics
TypeBlog Post...post, we talked about Addgene’s data processing needs, our criteria for selecting a new workflow management... -
#DeckTheLab to Win a Tasty Winter Treat This Holiday Season
TypeBlog Post...That will warm up the entire lab (hint: you might need some mini marshmallows…). We’ll choose 4 submissions...