Skip to main content
. 2018 Nov 2;9:4600. doi: 10.1038/s41467-018-06833-7

Fig. 2.

Fig. 2

Isolation of the causative lesion and expression pattern of Myh10. a Integrative genomics viewer (IGV) snapshot of the c.T1373G mutation in Myh10 (chr 11:68,765,165). b Normalized melting curves showing the Myh10 mutation by high-resolution melting analysis (HRMA). c Chromatogram of two different genotypes of Myh10 by Sanger sequencing. d Schematic diagram of MYH10 protein domains and the relative position of the L458 residue, which is conserved from worms to humans. e In situ hybridization for Myh10 expression in E13.5 whole-mount and on cryosectioned lungs; e epithelium. f Double staining for Tbx4 mRNA (red) and MYH10 protein (green) on E16.5 lung sections; e epithelium. g Immunostaining for MYH10, E-cadherin (marking epithelial cells), α-SMA (marking myofibroblasts and smooth muscle cells), PDGFR-β (marking myofibroblasts and smooth muscle cells), and NG2 (marking pericyte-like cells) on E16.5 and E18.5 lung sections; b blood vessel. Scale bars: 200 μm (e (left)), 50 μm (e (right), f (left)), 20 μm (f (right), g (left)), 10 μm (g (right))