We narrowed to 841 results for: Abo;

...therapeutic.” There are many fundamental questions about CRISPR/Cas biology still left to answer as well,...

...Additional Resources on the Addgene Blog Learn about other Fluorescent Biosensors A Practical Approach...

...diluting - if you end up concentrating your AAV above your desired titer and want to dilute it, err on...

...Additional Resources the Addgene Blog Learn More about SunTag Catch up on Your GFP Background Choose the...

... use the Gal4/UAS system, and you can read more about them in review articles (2–4). You can also take...

...return the sample back to the original pH. What about putting it back in the freezer? We then tested whether...

... with plasmids deposited at Addgene – typically about four times as many as papers without plasmids deposited...

...the Addgene blog Download our CRISPR eBook Learn about fluorescent protein-based tools Read all CRISPR ...

...vectors 101 eBook Resources on Addgene.org Learn about Addgene's viral service Find viral protocols and...

... mitochondrial DNA disorders.” This document is about the popular technique incorrectly known as “three-parent...

... minutes of FUS.  Similar constructs to the one above can be made for expressing your favorite T-cell ...

... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here.    ...

... Additional Resources on the Addgene Blog Read About Other Hot Plasmid Technologies Read Other Synthetic...

...received his PhD in biophysics from UCSF in the laboratory of Ronald Vale, after which he was a fellow at...

...1kb ladder (lane 1) that has bands ranging from about 500bp to 10kb, with the 3.0kb fragment having increased...

...within 3-5 days and resistant colonies appear in about 10-14 days depending on how quickly your cells divide...

... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here. ...

... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here.  ...

...fluorophore for an experiment is easy, but what about those times you need more than one?   Multiplex ...

...all be important.  If we eliminate the problems above: unclear methods, QRPs, and small samples, then ...

...light-regulated two component systems designed by the Tabor lab. Which inducible promoter is right for me? Here...

...you are a structure junky who just wants to learn about Cas domains. CasPEDIA either directly has this information...

... view of traces corresponding to the dashed box above. The number of action potential (AP) spiking events...

... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here.    ...

...collection Find plasmids for your research  Learn about our viral service ...

...our CRISPR 101 blog posts Find more information about Cas proteins Download the CRISPR 101 eBook Resources...

...to high copy numbers. This creates a potential metabolic burden on the yeast cells. Some phenotypes may...

...indirect approach - which means it’s time to talk about secondary antibodies. While a primary antibody ...

...IREB2, which post-transcriptionally regulate iron metabolism pathway transcripts. By using RaPID, Ramanathan...

...degrade any protein. We are particularly excited about the dTAG system as we can use it to evaluate the...