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CRISPR-Cas12a base editors confer efficient multiplexed genome editing in rice.
Cheng Y, Zhang Y, Li G, Fang H, Sretenovic S, Fan A, Li J, Xu J, Que Q, Qi Y
Plant Commun. 2023 Apr 13:100601. doi: 10.1016/j.xplc.2023.100601.
PubMed Article

Plasmids from Article

ID Plasmid Purpose
195366pYPQ230-D156R (ttLbCas12a)A temperature-tolerant LbCas12a mutant (D156R), also known as ttLbCas12a
195367dpYPQ230-D156R-CBE1dLbCas12a-D156R based cytosine base editor, hA3A/Y130F fused to the N terminal of dLbCas12a-D156R with the linker of XTEN with 3xFLAG
195368dpYPQ230-D156R-CBE2dLbCas12a-D156R based cytosine base editor, hA3A/Y130F fused to the N terminal of dLbCas12a-D156R with the linker of XTEN
195369dpYPQ230-D156R-CBE4dLbCas12a-D156R based cytosine base editor, hA3A/Y130F fused to the N terminal of dLbCas12a-D156R with the linker of (GGGGS)x6
195370dpYPQ230-D156R-ABE4dLbCas12a-D156R based adenine base editor, ecTadA8e fused to the N terminal of dLbCas12a-D156R with the linker of (GGGGS)x6
195371dpYPQ230-D156R-ABE5dLbCas12a-D156R based adenine base editor, ecTadA8e fused to the N terminal of dLbCas12a-D156R with the linker of (GGGGS)x8
195569dpYPQ230-D156R-ABE8dLbCas12a-D156R based adenine base editor, ecTadA8e fused to the N terminal of dLbCas12a-D156R with the linker of (GSAGSAAGSGEF)x3

Antibodies from Article