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Enhancing CRISPR-Cas12a base editing in plants with LbCas12a variants and introns.

Cheng Y, Li G, Zhou M, Mandlik R, Wang D, Qi Y
J Integr Plant Biol. 2026 Apr 2. doi: 10.1111/jipb.70249. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
250716dpYPQ230-RRV-ABEdLbCas12a-RRV based adenine base editor, ecTadA8e fused to the N terminal of dLbCas12a-RRV with the linker of (GGGGS)x8
250718dpYPQ230-RRV-intron-ABEdLbCas12a-RRV-intron based adenine base editor, ecTadA8e fused to the N terminal of dLbCas12a-RRV-intron with the linker of (GGGGS)x8
250719dpYPQ230-RRV-intron-CBEdLbCas12a-RRV-intron based cytosine base editor, hA3A/Y130F fused to the N terminal of dLbCas12a-RRV-intron with the linker of (GGGGS)x6
250923pYPQ142-AtUBQ10Golden Gate recipient and Gateway entry vector; assembly of 2 gRNAs driven by AtUBQ10 promoter
250924pYPQ144-AtUBQ10-pTGolden Gate recipient and Gateway entry vector; assembly of 4 gRNAs driven by AtUBQ10 promoter
250985pYPQ143-AtUBQ10Golden Gate recipient and Gateway entry vector; assembly of 3 gRNAs driven by AtUBQ10 promoter

Antibodies from Article