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L26 assembles within the nucle(ol)us. Localization of L25-eGFP and L26A-eGFP upon induction of an NMD3 dominant-negative allele; rpl26 null cells expressing L25-eGFP or L26A-eGFP were transformed with the pRS316-GAL-NMD3Δ100 plasmid, and transformants were grown in the presence of raffinose (SRaf-Leu-Ura). Galactose was then added to fully induce the Nmd3Δ100 protein. The GFP signal was inspected by fluorescence microscopy after 24 h. Arrows point to nuclear fluorescence.
