We narrowed to 830 results for: EED
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TypeBlog Post...or C-terminal fusion based on your experimental needs. Equally important, before cloning you must consider...dark fusions is likely misfolded, blocked from proceeding through the secretory pathway, and retained in...
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Important Considerations in Optogenetics Behavioral Experiments
TypeBlog Post...neuronal activation and is a sufficient readout to proceed with your behavioral experiments. Comparison of... to use c-fos expression to get the evidence you need. For example, as shown in this study [3], hippocampal... -
Plasmids 101: E. coli Strains for Protein Expression
TypeBlog Post...commercial strains designed to avoid them. Why do I need an expression strain? Protein expression from high-copy...number plasmids and powerful promoters will greatly exceed that of any native host protein, using up valuable... -
Proximity Labeling: A Powerful Tool for Protein Complex Purification and Proteomic Mapping
TypeBlog Post...their biotinylation. The advantage of APEX is its speed, labeling neighboring proteins in minutes rather...developed in the Ting Lab in 2018 to increase the speed of proximity labeling by promiscuous biotin ligases... -
Fluorescent Proteins 101: GFP Fusion Proteins - Making the Right Connection
TypeBlog Post...In the mVenus-APT1, a lipidation motif, which is needed for Golgi localization, is occluded and therefore...circularly permuted yellow fluorescent proteins." Proceedings of the National Academy of Sciences 101.29 (2004... -
Viral Vectors 101: Integrase-Deficient Lentiviral Vectors
TypeBlog Post...Lentiviral vectors can be produced easily, without the need for time-consuming purification processes, and are...delivered to cells, the viral life cycle initially proceeds as usual. Reverse transcription of the transgene... -
New Optogenetic Tools for Cytoskeleton and Membrane Control
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... -
3 Tips to Improve HDR Efficiency for CRISPR Editing in Human Cells
TypeBlog Post... A,T or C – but avoid NAG) or guide RNA target (“seed”) sequence. The idea was that these “blocking mutations...locus you are editing, and if the blocking mutation needs to be silent. In our view, it’s always best to change... -
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... -
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. ... -
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... -
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... -
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... -
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 ... -
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... -
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... -
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... -
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... -
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...