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Practical method for targeted disruption of cilia-related genes by using CRISPR/Cas9-mediated homology-independent knock-in system.

Katoh Y, Michisaka S, Nozaki S, Funabashi T, Hirano T, Takei R, Nakayama K
Mol Biol Cell. 2017 Feb 8. pii: mbc.E17-01-0051. doi: 10.1091/mbc.E17-01-0051. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
80766pDonor-tBFP-NLS-NeoCustomizable donor vector for CRISPR/Cas9-mediated homology-independent knock-in system.
80767pDonor-tBFP-NLS-Neo (Universal)Universal donor vector for CRISPR/Cas9-mediated homology-independent knock-in system.
80768peSpCas9(1.1)-2×sgRNA (empty, donor)All-in-one vector for CRISPR/Cas9-mediated homology-independent knock-in system. The plasmid contains eSpCas9(1.1) and two sgRNA expression cassettes. The first gRNA cloning site is empty.
80769peSpCas9(1.1)-2×sgRNA (IFT88, donor)Expresses eSpCas9(1.1) and two sgRNAs. The first gRNA targets human IFT88 and the second gRNA targets a pDonor-tBFP-NLS-Neo (Universal).

Antibodies from Article