TL;DR
The findings suggest that transient trim25 knockdown may alleviate intracellular restriction of exogenous reporter expression in PAC2 and CST cells and may provide an affordable approach for improving molecular manipulation in selected fish cell systems.
It is demonstrated that considerable UCOE minimization can be achieved without markedly compromising anti-silencing activity, providing a potential vector-design advantage by reducing the regulatory cassette footprint and increasing available vector capacity.
A modern electroporation protocol and expression vectors which utilize luciferase and green and ruddy fluorescent proteins as columnist qualities and a vector containing an expression cassette planned to be focused on to the tubulin locus of the parasite are created.
A transposase‐mediated platform for stable microRNA (miRNA) expression in CHO cells is established and the first application of a DNA transposon system for long‐term miRNA genome integration is demonstrated, demonstrating the applicability of transposase systems beyond protein‐coding transgenes.
Cas9 ablation enabled restoration of CUL4B expression and function following introduction of a CUL4B expression plasmid, providing proof of concept for a broadly applicable approach to studying protein function through rescue experiments.
The knockout and re-expression platform provides a useful gene editing tool for primary T cells in fundamental research and immunotherapy development and can be used to generate gene-edited primary T cells for in vivo studies, such as the quantification of anti-tumor responses.
This protocol describes an optimized reverse-transfection method for the efficient delivery of modified messenger RNA (mRNA) into senescent human fibroblasts and provides a practical approach for transient mRNA delivery into senescent cells.
We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.
