We narrowed to 859 results for: STI;

...  I’m updating it regularly as people send me suggestions. The most useful parts of the Guide are probably...

...human-designed protein that was not based on any existing protein structures, called Top7. Figure...

...Michigan State University with the backing of a prestigious Fulbright Fellowship. Dr. Kwapata now works as...

...data until November 9, 2020. Between then and the posting of the blog post, we just received news of deposits...

...scientific adventures.  You can submit your name suggestions here or by using the hashtag #AntibodyMakesThree...

...and metabolism. Melina has worked at Genetics Institute in Cambridge, MA and Sequana Therapeutics in San...

... general counsel at a small start-up is very interesting. It’s very varied. There’s IP work to do, general...

...We've also added two viral vectors that can constitutively express JEDI-2P, deposited by the St-Pierre...

... many cell types, as CAG is a ubiquitous and constitutive promoter. Use this for doxycycline inducible...

...molecular identifiers, which can improve the statistical power of in vivo screens. Figure 1: Using...

...work was cited by others?)  Ready to submit?  Fantastic! The next 25 submissions will receive a 20% off...

...Global Plasmid Distribution Check out the List of Institutions that Deposit their Plasmids with Addgene ...

...with a DOI for citation. If you’re considering requesting an Addgene antibody, the Data Hub can help you...

...new CRISPR plasmids available at Addgene. We will still periodically focus on specific CRISPR plasmid tools...

...Check Out Angela Depace's Talk on "Precision and Plasticity in Mentoring" We'd like to thank Niroshi and...

...organizing such a great day, we look forward to hosting more students next year! Does your lab or organization...

...and we’ll have some herd immunity, which raises questions like “How do you start to bring people back to...

...Incompatibility by Leah Schiesow If you're thinking about hosting multiple plasmids in one cell, it might be that...

...obvious from our most requested plasmid, SpCas9 is still going strong as the basis for many genome editing...

...that always have the same recognition site but distinct sites where the enzyme will cut. You only need...