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Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia.

Ishida Y, Kobayashi T, Chiba S, Katoh Y, Nakayama K
Hum Mol Genet. 2021 Apr 26;30(3-4):213-225. doi: 10.1093/hmg/ddab034. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
162276pGEX6P1-mCherry-Nanobody (LaM-2)Expresses GST-tagged anti-mCherry Nanobody (LaM-2) in E. coli cells.
218735pEGFP-C1-IFT43Expresses N-terminally EGFP-tagged IFT43 in mammalian cells

Antibodies from Article