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Bacterial Retrons Enable Precise Gene Editing in Human Cells.

Zhao B, Chen SA, Lee J, Fraser HB
CRISPR J. 2022 Jan 24. doi: 10.1089/crispr.2021.0065. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
170182pBZ186-pU6-(BbsI)_CBh-sv40NLS-Cas9-NLS T2A-mCherryMammalian expression vector for sgRNAs cloned into the BbsI sites and for expression of spCas9 linked to mCherry via a T2A peptide
170183pBZ191-pU6-sgBFP-CBh-sv40NLS-Cas9-NLS-T2A-mCherryExpression vector for a sgRNA against BFP and spCas9 linked to mCherry via a T2A peptide
170184pBZ202-pU6-sgBFP-An_CBh-sv40NLS-Cas9-Sa163RT-NLS-T2A-mCherryExpression vector for a sgRNA against BFP and spCas9-Sa163 RT fusion protein linked to mCherry via a T2A peptide. Donor template An was inserted in the Retron Sa163 msr-msd region by SpeI and AvrII.
170185pBZ210-pU6-sgBFP-An_CBh-sv40NLS-Cas9-Ec86RT-NLS-T2A-mCherryExpression vector for a sgRNA against BFP and spCas9-Ec86 RT fusion protein linked to mCherry via a T2A peptide. Donor template An was inserted in the Retron Ec86 msr-msd region by SpeI and AvrII.

Antibodies from Article