We narrowed to 893 results for: IND

... provide detailed evidence of knowledge new to mankind. And you probably understand how much faster it...class. Even so, it’s quite easy (and common!) to be blind to the cognitive load you’re placing on your audience... as pausing or turning off the slide deck (or reminding them to put their phones away), or maybe I was...

...do to combat this issue. First and foremost, be mindful of your extractions- if you need really clean RNA...blog Read blog posts related to plasmid protocols Find protocols for purifying DNA without a kit Resources...Addgene.org Check out our molecular biology protocols Find protocol videos on our website Read our Molecular...

...contributed by guest blogger Londa Schiebinger, PhD, Hinds Professor of History of Science, Stanford University...most of the results were positive, the analysis did find 263,000 more osteoporotic fractures. The overall.... To remedy this, Shah et al. provide a table indicating the sex of the most commonly used cell lines ...

...You can create an almost limitless number of DNA binding proteins with Cas9 guided by different promoters...large as natural regulatory networks. Addgene: What kinds of things could we do as genetic circuits become...  Thank you to Chris Voigt for speaking with us! Find the Plasmids: Plasmids for multi-input CRISPR/Cas9...

...Potential points where DNA errors can be introduced, indicated by exclamation marks. Error points include places... frame shifts, missing elements, and nucleotide indels or mismatches in significant plasmid elements. ...bioinformatics. Through their efforts, the QC team finds errors in 30% of deposited plasmids! We are committed...

...nature20149 Jiang Q, Meng X, Meng L, et al. Small indels induced by CRISPR/Cas9 in the 5’ region of microRNA... unexpectedly affect nearby genes (Figure 1A-C). Find CRISPR plasmids at Addgene! Knock-in: Introducing...

...editing!  CRISPR functions in use But exactly what kind of editing are people doing with all these CRISPR... modifier. We used these categories to see what kinds of CRISPR tools people were depositing and requesting... and the longevity of tools seen in Figure 3, indicates that the usefulness of popular CRISPR tools is...

...from and unique single stranded DNA primers that bind upstream (5’) and downstream (3’) of the DNA region...polymerase is also stable at this temperature and can bind to the primers.  Extension- The temperature is then... can learn all about ddPCR for AAV titration and find helpful tips and tricks in our blog post “Droplet...

...appropriate? If you already have an end product in mind, steps 1 and 2 will generally be straightforward...links to a CRISPR forum where you may be able to find information regarding your system of choice. The...driving Cas9 expression can be constitutive or inducible. U6 promoter is typically used for gRNA. May contain...

...(Figure 1B). The A260/230 ratio can be a good indicator of protein contamination, but a number of other...researchers traditionally use the A260/280 ratio as an indicator of protein contamination. However, this ratio ...used during nucleic acid purification can leave behind a variety of potential contaminants, some of which...

...supernatant containing antibodies. The antibodies bind the immobilized ligands and can be eluted once the...are incubated with the cell suspension. Antibodies bind ligands on the beads and a magnet is used to separate...Recombinant antibodies should be validated to ensure they bind their antigens specifically. Possible applications...

...are also available (Weigel and Glazebrook, 2002). Find plant plasmid resources at Addgene  Choosing an ...background growth of non-transformants and make finding true transformants more difficult. Don’t leave...arabidopsis in the classroom Resources on Addgene.org Find plant plasmids Visit our plant resource page Deposit...

...techniques Find tips on gRNA design Resources on Addgene.org Browse all CRISPR plasmids Find validated... and stability of the Cas9 protein in the host. Indeed, research has shown that a Cas9 protein from Geobacillus...

...networking at the time, but that means it was the best kind of networking! Since nearly every talk I’ve given...their interest. I won’t claim that I blew their minds, but I think many of the students learned something...Addgene.org Check out our comprehensive CRISPR guide Find CRISPR plasmids and resources ...

...their diverse utility, DNA transposons have been hindered by their limited programmability: depending on... crRNA, QCascade complexes survey the genome and bind target DNA sequences using RNA-DNA base pairing....Resources on Addgene.org Visit the CRISPR guide Find CRISPR plasmids for bacteria ...

...these frustrating and often months-long quests to find the right AAV for your system or to successfully...improve our Addgene Data Hub, 76% of respondents indicated they wanted to see more negative data (Figure ... e-book Additional Resources on the Addgene Blog Find and Share AAV Data with Addgene's New AAV Data HubCelebrate...

...complementary to the DNA target. The 20-nt guide region binds to the DNA sequence immediately downstream of the...ICAR-Central National Rice Research Institute in India. He specializes in genome editing tools with a focus...F. (2019). Plant gene editing through de novo induction of meristems. Nature Biotechnology, 38(1), 84–...

...world has been long-read sequencing. Whereas the individual reads generated in short-read and Sanger sequencing...base identity and plasmid length. Any mismatch or indel flags the sequence for manual review by one of our... QC Process Bioinformatics at Addgene The Power Behind NGS Plasmid Validation: seqWell Addgene’s Tips ...

...visually select cells in a microscopy image for individual analysis. A shuttle vector designed for this ...plasmids are those that can replicate in multiple kinds of bacteria, including many natural plasmids. By... same molecular language as the tree outside my window! Whatever you use them for, shuttle vectors can...

...that! I organized my lab data so well that I can find the results of any experiment I’ve run in under ...format regardless of whether you’re in academia, industry, or nonprofits. Like any other letter, they have...Our Management for Scientists Series Get Tips on Finding Your Perfect Job after Graduation Additional Resources...