This customizable lentiviral vector will allow you to successfully deliver your gRNA sequence to the target cell of interest, under the control of the U6 promoter. Using the CRISPR-Cas9 system, you can target and modify DNA sequences of interest.
Examples of Applications
- Use for CRISPR-Cas9 genome editing technology
- Use with Lenti-ONE Cas9 for a two-vector CRISPR System