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A scalable CRISPR-Cas9 gene editing system facilitates CRISPR screens in the malaria parasite Plasmodium berghei

Jonsdottir TK, Paoletta MS, Ishizaki T, Hernandez S, Ivanova M, Curbelo AH, Saiki PA, Selinger M, Das D, Henriksson J, Bushell ESC
bioRxiv 2024.04.20.590404 (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
216421pPbHiT_3xmyc_hsp70UTR_hdhfr/yfcuEmpty backbone to express gene specific gRNA and carry the homology repair template for CRISPR editing of Plasmodium berghei using the PbHiT system.
216422pPbU6_hdhfr/yfcuEmpty backbone to express gene specific gRNA from the Plasmodium berghei U6 promoter for traditional CRISPR editing.
216423pPbU6_hdhfr/yfcu_Cas9Empty backbone to express gene specific gRNA from the Plasmodium berghei U6 promoter and the Cas9 nuclease for traditional CRISPR editing.

Antibodies from Article