We narrowed to 1,049 results for: ins

...CRISPR than just designing a repair template that contains your desired edit, and I want to make sure that...long ssDNA template to increase efficiency of insertion and gene replacement. Care to share your favorite...

...libraries In surface display, proteins of interest are fused to anchoring proteins to be expressed on the surface...

...Instead of spending time and money producing virus from select vectors in the repository yourself, you...serotypes that can be used to deliver fluorescent proteins to cells as determined by the serotype. You can...

...embryogenesis. My interests, though, have proven unruly. Instead of settling down into a singular focus on molecular... general terms on a couple of very broad topic domains, but each day brings in new and surprisingly diverse...

...natural or synthetic, the researchers looked at intrinsic properties (GC content or rare codon percentage...not rare codons and many genes where there are instances of rare codons, sometimes intentionally modulating...

...field of science you are communicating from. For instance, a plumber, a physicist, an ambassador to Spain...exclude people outside of the original recipients. Instead, it targets a specific audience - giving consistency...

...recombinase competition Article contributed by Aliyah Weinstein Sparse Predictive Activity through Recombinase...protein fusions with tTALE to “stain” DNA. TALE proteins can bind specific DNA sequences which brings the...

...partnerships with universities, companies, hospital institutions and funding bodies. Don't shy away from the ...company advancement. Be relentless The world is against you.  As I mentioned, you start at a disadvantage...

...models for immunogenicity prediction of therapeutic proteins. European journal of pharmaceutics and biopharmaceutics...biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 130, ...

...reading through a paper to find that there is insufficient information about which reagents were used? ... options using the different PID formats The instructions for how to cite any Addgene plasmid in your ...

...help unlock the potential of modern sequencing instruments by enhancing the efficiency and simplicity of...completely unnecessary for sequencing multi-kb DNA inserts and larger targets. The NGS readout also reveals...

... the DNA prep is larger. And since the library contains many plasmids, care must be taken to ensure that...plasmids in the library are identical except for the insert; there’s no need to sequence other parts of the...

...never finish a course of antibiotics, choosing instead to save a few days’ worth of capsules to self-medicate...much of the information gained from that research remains inaccessible, behind paywalls and in technical ...

... Figure 1: Can you draw Spongebob from these instructions without knowing you're suppose to draw Spongebob..., test out the technology before the conference begins.“There were some concerns of having a stable internet...

...need to present yourself using a resume. Indeed, instead of having all the pages in a Curricula Vitae to...career, she transitioned into a communications role instead after she completed her MSc in Experimental Medicine...

...vector developed by Feng Zhang’s lab at the Broad Institute (Sanjana et al., 2014). It is a dual-vector system...viruses are popular, pAAV-hSyn-DIO-hM4D(Gi)-mCherry contains a double floxed human muscarinic receptor 4 (Gαi-coupled...

...lengths. Recent alternatives to Cas9 While Cas9 remains the most widely used CRISPR nuclease, recent work...101 blog posts Find more information about Cas proteins Download the CRISPR 101 eBook Resources on Addgene.org...

.... Projects such as the OpenFlexure Microscope (Collins, et. al., 2020), the miCube, SQUID (Hongquan, et...and low-cost optical setups. References Joel T. Collins, Joe Knapper, Julian Stirling, et. al, "Robotic...

... coexpression of light (green) and heavy (blue) chains as driven by two CMV promoters (orange). Figure... to WGS the lab’s entire hybridoma collection. Instead, the Trimmer Lab moved to direct functional validation...

...for your workflow. Next time you make a mistake, instead of silently vowing never to do that again (I’ve...incubation periods to have another short "quiet period" instead of immediately running to the next thing.  It may...