We narrowed to 629 results for: Dos

...science.1138389 Le TTH, Tran NT, Dao TML, Nguyen DD, Do HD, Ha TL, Kühn R, Nguyen TL, Rajewsky K, Chu VT ...off-target editing, and, for RNA editing, fine-tuning dosage so that enough wild-type MECP2 is made inside the...

...saturation mutagenesis with the same protocol. What do you think about one pot saturation mutagenesis? How...

...clinical grade hiPSCs, reprogramming methods that do not involve modification of the original genome by...

...caption courtesy of Challis et al., 2022. Where do they come from? Systemic capsids are typically derived...efficacy can vary depending on species. LY6A and LY6C1 do not have known homologs in NHPs, and capsids that...mouse strains). AAV-PHP.eC, AAV9-X1.1 and AAV1-X1 do not display strain-specific tropism and can be used...2023). High viral titer High vector genome (vg) doses are recommended for all systemic capsid applications... AAV-PHP.eB is typically administered at a total dose between 1 x 1011 and 5 x 1011 vg per animal (i.e...mL titer), while AAV-PHP.S is typically used at a dose between 3 x 1011 and 1 x 1012 vg*. Most systemic...capsids are easy to produce in high titer, but higher doses (>1 x 1012 vg total in mice) may increase the chances...

...tested with AYBEv3!). Although AYBE, AXBE, and ACBE do not approach the high product purity of CBEs and ...

...processes in different cell types. One great way to do this is to use CRY2-CIB1 clustering. Fuse either ...provided CIB constructs for targeting Golgi, ER, and endosome membranes) (Figure 4). The authors used SuperPLD...

..., phosphomimetic mutations on the activation loop do not fully activate MEK1. In fact, replacing just ...

...comparison. These next-generation sequencing techniques do not typically rely on Sanger sequencing but instead...

...utmost priority for countries around the world and to do so, the WHO recommends one strategy: testing, tracking...Servellita V, Singh J, Miao X, Streithorst JA, Granados A, Sotomayor-Gonzalez A, Zorn K, Gopez A, Hsu ...

...negative selection markers for allelic exchange. To do this, we performed the following modifications to...

...your target base in the protospacer sequence. If you do not find a suitable ‘NGG’ PAM at your target genomic...

... by restriction enzyme cloning, you would have to do it in two steps, and a scar would likely remain between...

...default state. In contrast, Brainbow-3.1 and -3.2 do not display default fluorescence due to the addition...

...surface epitopes for many proteins, but some proteins do not have such epitopes. These classical 'undruggable... to track endogenous activity of EGFR, including dose-dependent response to EGF (Promega, 2025). The value...diminished luminescence signal, associated with endosomal localization of EGFR. This method offered kinetic...

...systems listed above are orthogonal, meaning that they do not affect each other. For example, the GAL4 transcription...

...near optimal wavelengths (Fluc emits at 610 nm) and do not require external light sources. Unfortunately...

...success, we find it is usually faster and easier to do the validation first.  AAV-mediated gene expression...

...you’ve introduced your RNAi into your organism, how do you identify the actively silenced ones? Here, I’...

...recombinant clones are generated.  A simple way to do this is to express lambda red genes from a plasmid...

...μm) tissue sections and 3D cultures These samples do not necessarily require optical sectioning, but open...while also avoiding the toxic effects of high light doses to the cells. Thin static samples Ex: Fixed monolayers...out of focus light. However, they also continually dose the sample from top to bottom with excitation light...