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...exceptions to our standard workflow.  Table 1: Guidelines for the data fields in the deposit spreadsheet...

...scientists must genotype each animal to identify the ones with the desired genotype. Inducible and conditional...

...something that made them better than my unsuccessful ones. With grant applications there’s going to be an ...

... Abcam and NEB have Ph.D.s answering emails and phones). We can’t be experts on every technique or experiment...

...orientation, and type of target sites that flox your genes of interest, a powerful FLEx switch can be created...

...best performer mGold — while maintaining high brightness and fast maturation time (Figure 1). See the ...

...G., Künne, T., . . . Sternberg, S. H. (2019). Harnessing type I CRISPR–Cas systems for genome engineering...

...McCawley, P. (1977). The establishment of two cell lines from the insectspodoptera frugiperda (lepidoptera...

...photobleaching, lack of red-shifted indicators, and brightness of fluorescence all have room for improvement...

...to run larger panels: five laser spectral flow machines have 64 detectors, allowing for the use of up ...

...Coloc 2, BioImageXD, and customized CellProfiler pipelines. Image analysis software produces quantifiable...

...BioMolecular Modeling, we spun off a small, family-run business – 3D Molecular Designs – to commercialize some...

...these expected hits, we always get hits to “random” genes. Do these hits always mean the sample is contaminated...

...the expected complete sequence for the lacI/lacZ genes (1), while sequencing of white colonies showed a...

...interview or campus visit in person, things like sickness or scheduling issues can and do interfere with...

...inconvenient. Another possible reason for the trickiness of NgAgo is the inability of mature NgAgo protein...

...science outreach: engaging the public to promote an awareness and understanding of science. Like most science...

...you like to bring your phone in the lab, though, honestly, this still grosses me out. Maybe it’s just me...

...website to verify plasmids or validating your new clones, try these tips to make the most of your time and...

... of the mean rate for each paper. Green and red lines depict the sum of mean +1 and -1 std for each paper...