Research Article
SLC26A4 Mutation Promotes Cell Apoptosis by Inducing Pendrin Transfer, Reducing Cl- Transport, and Inhibiting PI3K/Akt/mTOR Pathway
Figure 1
Sequence electropherograms and measurements of GFP and SLC26A4. (a) Mutant 1 of SLC26A4 (c.85G>A) and its corresponding wild-type sequence. (b) Mutant 2 of SLC26A4 (c.2006A>T) and its corresponding wild-type sequence. (c) Mutant 3 of SLC26A4 (c.853G>A) and its corresponding wild-type sequence. Arrows showed mutation sites in SLC26A4. (d) GFP fluorescence was observed under a fluorescence microscope after transient transfection. (e) GFP expression was determined by Western blot. GAPDH served as an internal control. (f) SLC26A4 expression was determined by qRT-PCR. GAPDH served as an internal control. &&Pā<0.01 compared to the control group. ## compared to the vector group.
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