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. 2016 Apr 23;7(21):31440–31453. doi: 10.18632/oncotarget.8951

Figure 2. NEDL1 is not critical for mice survival.

Figure 2

A. Schematic diagram of the generation of Nedl1−/− mice. Nedl1 mutant mice were generated from a C57BL/6J ES clone carrying the targeted Nedl1 allele designed to allow Cre-mediated deletion. Mice carrying the targeted Nedl1 allele were bred to EIIa-Cre transgenic mice to remove the neor gene and generate Nedl1LacZ/+ reporter mice in which exon 8 are deleted and replaced with an IRES-LacZ gene. Offspring were intercrossed to generate homozygote Nedl1LacZ/LacZ (Nedl1−/−) mice. Exons are represented by blue boxes. B. Photograph of 18-month-old Nedl1+/+ and Nedl1−/− mice. C. ENS system detected by AChE-staining (upper panel) 2-month-old Nedl1+/+ mice and Nedl1−/− mice (Scale bar: 50 μm) and HE staining of kidneys (lower panel) from 6-month-old Nedl1+/+ mice and Nedl1−/− mice (Scale bar: 500 μm) show that there were no obvious defects in ENS and kidney. D. Analysis on HE staining of some tissue sections from 2-month-old Nedl1+/+ mice and Nedl1−/− mice. There were no obvious defects in brain, cerebellum, testis, heart, liver, spleen and lung. Scale bar: 50 μm.