We narrowed to 629 results for: Dos;

...students next year! Does your lab or organization do work to help improve K-12 education? Let us know ...

...less likely to alter a protein’s properties. Why do we need new epitope tags? Short epitope tags like...

...alone. (Seriously, is there anything CRISPRs can't do?) Structural details All this, and scientists are...

...of people willing to make that idea a reality! How do you share your science with the community? Addgene...

...it. 6. Edit your DNA sequence Finally, when you do see a miscalled peak, don’t be shy. Feel free to ...

...available through Addgene, and they hope others will do the same. “This isn’t the final version,” she said...

...tools in C. elegans and in Plasmodium. For those who do want to apply LITEs for the transformation of neurons...exposure. Third, the response can be graded with light dose and is fully reversible after light retraction. ...

...selection: labeling markers that your cells of interest do not have, and selecting for the cells that are not...cytosolic proteins alongside the intranuclear ones. You do not need to use a separate fix/perm cytosolic procedure...

... a single gene to cells. Still in bacteria, which do not produce BV, an additional gene coding for heme...proximity of the N- and C-termini. Latest miRFPnanos9 do not yield to (m)iRFPs in cellular and molecular brightness...

...GFP, or RFP. Cells that express the construct but do not undergo recombination can be detected by immunostaining...transgene expressing either YFP or CFP, and cells that do not express Cre fluorescing with the default RFP....