...variety of applications. While editing this post, I learned a lot about how FRET can be used to study biological...

... year we’d like to know what topics you want to learn more about. Our post on “Making Your Own Competent...

...you have information or another resource to add, please tell us about it in the comments. ...

...relevant variants. This list is not exhaustive - please browse our curated list of opsins here to find ...of a protein of interest. A genetically-encoded nuclear Cry2 fusion can thus direct a CIB1-protein fusion...voltage (LOV) domain of FKF1 LINUS light-inducible nuclear localization signal based on the LOV2 domain of...phototropin 1 LOVETRAP reversibly sequester and release proteins from cellular membranes using light. light-induced...protein in the light ~400 (on)/~500 (off) PhoCl Photocleavable protein engineered from a green-to-red photoconvertible...

...plasmid cloning Read our Plasmids 101 blog posts Learn about the differences between transformation, transduction...

...links to articles citing this plasmid. Now you can learn how a plasmid has been used by multiple labs and...

... click here to register and join your postdoc colleagues in envisioning the Future of Science. Attend...

...'t wait until you need a job to meet people and learn about what's out there.”- Joanne Kamens, Executive...

... found that our competent cells are good for at least a year when stored at -80oC.   For each new batch...

...included in the next What’s New in CRISPR blog post, please let us know. We also welcome blog posts from guest...

... AAV prep for the 2nd year running, and you can learn more about this useful, DREADD-containing AAV here...

...'re accelerating the future of science. Want to learn more about our latest developments? Subscribe to...

... deposit also includes pXPR_071, a plasmid that leads to higher titer lentivirus preparations than the...

....    Additional Resources on the Addgene Blog Learn About Experimenting in an Open Source Lab Resources...

...and easy ways to share your documents with your colleagues. Start small by identifying the protocols, guides...

...your screen. If you need to amplify the library, please refer to the depositor’s protocol for the best ... library is complete - an incomplete library may lead to false positives or false negatives in later experiments...minimizes the effects of random chance that could lead to false positive or negative results - for a given...sequencing services. For an NGS company near you, please consult these links: NGS Company Resources Science...

...included in the next What’s New in CRISPR blog post, please let us know. We also welcome blog posts from guest...

...inhibitory feedback in response to norepinephrine release, and clinically-used drugs targeting these receptors...

...to observe what’s happening inside cells for at least a couple of decades. Green is the classic color,...

...29300010. Additional Resources on the Addgene Blog Learn more about in vivo imaging tools The luciferase ...