Fig. 5 | Scientific Reports

Fig. 5

From: Identification and functional study of a novel FOXC1 missense mutation in a Chinese family with Axenfeld–Rieger syndrome

Fig. 5

FOXC1-WT and FOXC1-H128Y expression. Western blot analysis revealed that the protein level of FOXC1-H128Y was lower than that of FOXC1-WT. (A) Total cell lysates from transfected HEK293T cells were subjected to western blot analysis. (B) Bar chart showing FOXC1-WT and FOXC1-H128Y protein expression levels (n = 4 independent experiments, p < 0.05 as determined by the Mann‒Whitney test, means ± SEs).

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