/
/
Construction of CRISPR Plasmids and Detection of Knockout Efficiency in Mammalian Cells through a Dual Luciferase Reporter System
É necessária uma assinatura da JoVE para visualizar este conteúdo. Faça login ou comece sua avaliação gratuita.
Capítulos
- 00:05Introduction
- 00:45Oligonucleotide Annealing and sgRNA/CRISPR Vector Digestion
- 01:51Identification of the Correct Recombinant Plasmids by PCR
- 02:42Dual-luciferase Detection
- 04:16Results: Design of sgRNA to Target Sheep DKK2 Exon 1
- 05:20Conclusion
Here, we present a protocol describing a streamlined method for the efficient generation of plasmids expressing both the CRISPR enzyme and associated single guide RNA (sgRNAs). Co-transfection of mammalian cells with this sgRNA/CRISPR vector and a dual luciferase reporter vector that examines double-strand break repair allows evaluation of knockout efficiency.
