We narrowed to 798 results for: KIN

...riboregulation could be a promising strategy for linking RSM inputs to endogenous gene expression (2). ...terminators, promoters, and genes) were built with flanking primer binding sites (designed to have 20-30 nt...

...gRNAs to choose from. With so many possibilities, picking a gRNA with an optimized sequence is of primary...detectable mutations (Veres et al., 2014). When working with single-cell clones, the authors note that ...

...with DIO/FLEx vectors and off-target expression making it easier to determine the spread pattern around...false negative or conclude the viral vector is not working.  When using a “cell-type specific” promoter, such...

...mutations are essential data points for investigators looking to definitively link genotype and phenotype. It... and do not require high sequencing read counts making them fast and viable options for multiplex sequencing...

...photographer at the Super Bowl, a medical technologist taking an x-ray, or a biologist imaging the smallest structures...microscope to use for a new sample I always start by asking two questions: 1) Is the sample dynamic or static...

...cytometry particularly well to complex experiments looking at a variety of different targets. If you are planning...43:404–409 . https://doi.org/10.1063/1.1685647 McKinnon KM (2018) Flow Cytometry: An Overview. Current...

...Base editors chemically modify DNA bases without breaking the DNA backbone, sidestepping the problem of ... 98-99% target modification in primary T cells, making them a promising tool for cell therapy applications...

...efficiency is so high that some applications may permit working with edited “pools” of cells, eliminating the time-consuming...telomere length. Telomere trimming can be assayed by looking for the production of ECT-DNA (extra-chromosomal...

...Looking for a fast and inexpensive way to determine your antibody's purity? Check out our latest protocol...

...Thinking about using antibody-based applications in your experiment...but not sure where to start or ...