Morphofunctional and Biochemical Approaches for Studying Mitochondrial Changes during Myoblasts Differentiation

Figure 2

Confocal microscopy of C2C12 myoblasts (a–d) and late myotubes (e–h), after Mito Tracker (a, b, e, f) and JC-1 (c, d, g, h) staining. Graphs of lower panel show the different fluorescence JC-1 intensity in myoblasts (i) and late myotubes (j). (a–h): Bar=20 μm.

(a)

(b)

(c)

(d)

(e)

(f)

(g)

(h)

(i)

(j)