Skip to main content
Fig. 5 | BMC Medical Genetics

Fig. 5

From: Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer

Fig. 5

To analyse the impact of the patient mutation on the protein level, HEK293T cells expressing FLCN WT or Mut fused to GFP using the TALEN technology were generated. a and b Western blot analyses reveals that the mutant protein is hardly expressed. This could in part be alleviated with MG-132 (a, treatment with 10 μM for 2 h) or chloroquine (b, treatment with 50 μM for 24 h), indicating an involvement of the proteasome and lysosome in the degradation process. Tubulin served as loading control (p =3, error bars indicate SEM, * = p < 0.05, n.s. = not significant, two tailed t-test)

Back to article page