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. 2020 Nov 26;21(23):8981. doi: 10.3390/ijms21238981

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© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Immunoblot of GLUT4, Rab8A, Rab13, and Rab14 in the isolated rat soleus muscle proteins. Cell lysate proteins (50 µg) were immunoblotted using β-actin as the loading control. (a) Representative Western blot images of the target proteins. (b) The expression of GLUT4, Rab8A, Rab13, and Rab14 are shown at the normalized expression level of DM. For each group, values are presented as the mean ± SD of six rats per group. One-way ANOVA followed by the post hoc Scheffé test were used for the statistical analysis: * p < 0.05 and *** p < 0.001.

Immunoblot of GLUT4, Rab8A, Rab13, and Rab14 in the isolated rat soleus muscle proteins. Cell lysate proteins (50 µg) were immunoblotted using β-actin as the loading control. (a) Representative Western blot images of the target proteins. (b) The expression of GLUT4, Rab8A, Rab13, and Rab14 are shown at the normalized expression level of DM. For each group, values are presented as the mean ± SD of six rats per group. One-way ANOVA followed by the post hoc Scheffé test were used for the statistical analysis: * p < 0.05 and *** p < 0.001.