Hassle-free 96-well Format Epitope Tagging Using Cas9 Ribonucleoprotein
Type
Blog Post
Published
June 28, 2018, 3:01 p.m.
...to the template strand. Therefore, I suggest that picking a crRNA complementary to the template strand...bound by a protein of interest are pulled-down and later coupled to high-throughput sequencing to identify...optimized to achieve high knock-in efficiency.
To calculate the tagging efficiency in the transfected cells...tagging experiments by assembling csRNPs in a 96-well plate format and tested parallel tag knock-in for 96 different...single go (Figure 3). We were able to tag >30 genes/plate in the first shot with typical knock-in efficiencies...knock-in experiment were pre-assembled in a 96-well plate. Glioma stem cells were transfected in 96-well format...device; 5 days after the transfection, the entire plate was scanned for V5 tagging using an Operetta imaging...