We narrowed to 933 results for: KIN

...membrane-bound spike protein, in a remarkable 12 working days. While the lab used this method for COVID-...

...relative quantification - that is, since you’re looking at the amount of DNA in your sample relative to...

...round of evolution (AID-2) to reduce some of the leakiness associated with the system, but the general concept...

...been limited, in part, due to the necessity for working with this virus under the highest biosafety level...

...Multi-color labeling of neurons is for more than making pretty pictures (see figure 4). It also enables...

...phenotypic analysis it is appropriate to begin working in the T2 generation. The selection process itself...

... Addgene Blog Read this blog post about CRISPR Kinome Libraries available at Addgene Learn about the ...

...array. Workflow and technical considerations Making insertions in bacterial genomes with the V. cholera...

...resources References Bauzon, M., Castro, D., Karr, M., Hawkins, L. K., & Hermiston, T. W. (2003). Multigene expression...

...complex trendlines. If you don’t have access to this kind of software, don’t give up! Rather than plotting...

...neuron-specific promoters, including calmodulin-dependent kinase II alpha (aCaMKII; excitatory neurons) and Synapsin...

... repaired by cellular mismatch repair machinery making an original C-G pair converted to T-A or reverted...

...So, as long as it doesn't look done, just keep working on it. Also bear in mind that this is just a review...

...through a second recombination event between the two flanking repeats. In cells where recombination has not ...

...Cas13 enzymes require a single base protospacer flanking sequence (PFS) adjacent to the target, but many...

...APOBEC-Cas9 editosome would restore eGFP fluorescence, making it easy to quantify single base editing efficiency...

... version of TnpB is just 408 amino acids long — making it one of the most compact genome editors to date...

...choose the best method based on the plasmid. By working with the Data team, the QC team has also improved...

...assembly of the split luciferase is reversible, making PILATeS suitable for live imaging with a time resolution...

...results can be compared; results from an experiment lacking the proper controls are invariably inconclusive...