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Molecular basis underlying the ciliary defects caused by IFT52 variations found in skeletal ciliopathies.

Ishida Y, Tasaki K, Katoh Y, Nakayama K
Mol Biol Cell. 2022 Aug 1;33(9):ar83. doi: 10.1091/mbc.E22-05-0188. Epub 2022 Jun 15. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
218732pCAG-EGFP-C-IFT81Expresses N-terminally EGFP-tagged IFT81 in mammalian cells
218733pCAG-EGFP-C-IFT88Expresses N-terminally EGFP-tagged IFT88 in mammalian cells

Antibodies from Article