Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
Type
Blog Post
Published
Dec. 10, 2020, 1 p.m.
... et al., 2015). In these studies, the strategy employed was to deliver a standard AdV vector to the targeted...AdV-mediated transduction of gRNA:Cas9 ribonucleoprotein complexes into transformed and non-transformed cells yielded...genes. For this you would need to provide a DNA template to repair the double strand break via homology...Cas9/sgRNA and one vector for your specific DNA template. Using this two vectors system, Manuel Gonçalves...a potential platform that could be realized via simple switching of the relevant gRNAs and donor DNA
Adenoviral...tools can also be used to deliver Cas9 and DNA templates in somatic cells of adult animals in order to ...vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array...