CRISPR 101: Mammalian Expression Systems and Delivery Methods
Type
Blog Post
Published
Sept. 24, 2015, 2:30 p.m.
...elements are inserted into an AAV transfer vector and used to generate AAV particles.
Transient or stable... in a single lentiviral transfer vector or separate transfer vectors. May contain reporter gene (e.g. ...non-dividing cells. AAV is least toxic method for in vivo viral delivery.
Cas9 mRNA and gRNA
Plasmids containing...add a tag, you will also need to deliver a donor plasmid or single-stranded DNA oligonucleotide, so you ...Components of System
Application
Mammalian expression vector
Promoter driving Cas9 expression can be constitutive...generate stable cell lines. Packaging and Envelope plasmids provide the necessary components to make lentiviral...for conducting genome-wide screens using CRISPR.
AAV transduction
Only compatible with SaCas9 (packaging...