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Transient inhibition of p53 enhances prime editing and cytosine base-editing efficiencies in human pluripotent stem cells.

Li M, Zhong A, Wu Y, Sidharta M, Beaury M, Zhao X, Studer L, Zhou T
Nat Commun. 2022 Oct 27;13(1):6354. doi: 10.1038/s41467-022-34045-7. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
196582pCMV-PE2-p53DDMammalian expression of SpCas9 prime editor 2 with P2A-p53DD
199267pEF_PE2Mammalian expression of SpCas9 prime editor 2 under EF1α promoter
199271pegRNA-GBA-10pegRNA used to induce GBA (c. 1226 A > G) mutation
199272pegRNA_LRRK2-3pegRNA used to induce LRRK2 (c. 6055 G > A) mutation
199273pegRNA_LMNA-1pegRNA used to induce LMNA (c.1824C > T) mutation
199274pegRNA_GBA-4pegRNA used to correct GBA (c. 1226 A > G) mutation
199275pegRNA_LMNA_CR-2-5pegRNA used to correct LMNA (c.1824C > T) mutation
199276Lsg-GBA-1 + 2nicking sgRNA to induce or correct GBA (c. 1226 A > G) mutation using PE3
199277Lsg-LRRK2-1nicking sgRNA to induce LRRK2 (c. 6055 G > A) mutation using PE3
199278Lsg-LMNA-1 + 2nicking sgRNA to induce LMNA (c.1824C > T) mutation using PE3

Antibodies from Article