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Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA.

Richardson CD, Ray GJ, DeWitt MA, Curie GL, Corn JE
Nat Biotechnol. 2016 Jan 20. doi: 10.1038/nbt.3481. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
71820pCR1002Express Streptococcus pyogenes Cas9
71821pCR1003Express Streptococcus pyogenes dCas9 (D10A, H840A)
71822pCR1054Express Streptococcus pyogenes nCas9 (D10A) nickase carrying two C-terminal SV40 NLS
71823pCR1055Express Streptococcus pyogenes nCas9 (H840A) nickase carrying two C-terminal SV40 NLS
71824pCR1056Express Streptococcus pyogenes dCas9 (D10A, H840A) carrying two C-terminal SV40 NLS
71825BFP dest cloneLentiviral introduction of BFP reporter (Point mutation H66 in mEGFP results in BFP expression)

Antibodies from Article