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. 2021 Jul 2;11:13771. doi: 10.1038/s41598-021-93110-1

Figure 1.

Figure 1

Analysis of FYCO1 tissue distribution and generation of FYCO1 knockout mice. (A) Extracts from various 4-week-old male C57BL/6J mouse tissues and MEFs (30 μg of protein) were subjected to western blot analysis with anti-FYCO1 antibody. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as a loading control. This experiment was performed once using one mouse. (B) The mouse FYCO1 gene was disrupted by the insertion of a neomycin resistance gene cassette (Neo) in the first coding exon. Open and filled boxes represent coding and noncoding exons, respectively. The diphtheria toxin A gene cassette (DT-A) was inserted outside of the 3’ homologous region for negative selection. Restriction enzyme sites and probes used for Southern blot analysis are indicated. (C) Lysates from 4-week-old WT and KO mouse tissues (heart and brain) were subjected to western blot analysis with anti-FYCO1 antibody. This experiment was performed once using a mouse. (D) Lysates from 4-week-old WT and KO mouse tissues (eyes) were subjected to western blot analysis with anti-FYCO1 antibody. This experiment was performed once using a mouse.