We narrowed to 902 results for: Nes
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TypeBlog Post...discussed how the regulation of bacterial ORIs determines plasmid copy number within the bacterial cell...
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Will You Be My Mentor? Finding and Asking for Mentoring Support
TypeBlog Post...often have mentoring programs. The Healthcare Businesswomen’s Association hosts an excellent group mentoring... -
Summer SciComm Series: Cognitive Load
TypeBlog Post... the slide deck (or reminding them to put their phones away), or maybe I was assuming something was intuitive... -
Announcing the Winners of the 2021 Michael Davidson and Roger Tsien Commemorative Conference Awards
TypeBlog Post...fuses MPST to roGFP2. Because roGFP2 contains two cysteines near the chromophore that are susceptible to redox... -
Lighting Up Cell Signaling with Photoswitchable Kinases
TypeBlog Post...photoactivatable fluorescent proteins in empty backbones in the Michael Davidson Collection Find Photoswitchable... -
Choosing the B(right)est Fluorescent Protein: Photostability
TypeBlog Post...Additional Resources on Addgene.org Find Empty Backbones with Fluorescent Tags Find Plasmids for Subcellular... -
Troubleshooting Your Plasmid Cloning Experiment
TypeBlog Post...cloning strategy. Once you've identified potential clones after the screening, sequence the plasmid. Many... -
Visualizing Protein Turnover In Situ
TypeBlog Post... Professor Schuman’s lab showed that FUNCAT’s usefulness can be extended to determine the turnover of ... -
RNA Extraction Without A Kit
TypeBlog Post...all-in-one acid-guanidinium-phenol solution that combines the homogenization solution and phenol addition... -
Antibodies 101: Fab Fragments
TypeBlog Post...heavy chains. In the lab, this is the region that determines what secondary antibody you should use when performing... -
Giving gRNAs a Facelift - Synthetic and Beyond
TypeBlog Post...Some of these synthetic modifications, specifically ones which do not contain a 5’ triphosphate in the gRNA... -
Developing Lab Management Software for Biology
TypeBlog Post...how software can be structured to allow for the messiness of biology. These examples are intentionally trivial... -
The Future of Research Symposium Boston 2015
TypeBlog Post...generating too many trainees per PI” “Lack of awareness about how the system operates and functions” “... -
New Tool for Lineage Tracing: The ClonTracer Library
TypeBlog Post...limit of roughly 0.1%. Thus, rare, pre-existing clones that are present at less than 0.1% of the total... -
Plasmids 101: Cre-lox
TypeBlog Post...removal – in conventional mouse targeting, targeted clones are selected for using a resistance marker; however... -
Quickest Way to Deposit Plasmids: The Deposit Spreadsheet
TypeBlog Post...exceptions to our standard workflow. Table 1: Guidelines for the data fields in the deposit spreadsheet... -
Mouse Modeling, Part 1: Genetically Engineered Mice
TypeBlog Post...scientists must genotype each animal to identify the ones with the desired genotype. Inducible and conditional... -
Split-BioID: An Improved Method for Studying Protein-Protein Interactions
TypeBlog Post... via plasmids or by the creation of stable cell lines and these cells are then grown in biotin-containing... -
Lab Automation at Addgene
TypeBlog Post...t electronic but it is one of the most helpful machines I have used in the lab. It’s especially useful... -
High Complexity Golden Gate Assembly with NEB’s DAD
TypeBlog Post... 500 times the number of plaques than the linear ones. The 52-piece circular assembly of the T7 genome...