Skip to main content
. Author manuscript; available in PMC: 2010 Apr 1.
Published in final edited form as: J Neurosci Res. 2009 Apr;87(5):1250–1259. doi: 10.1002/jnr.21921

Fig. 3.

Fig. 3

Relative distribution of cypD in crude mitochondrial samples from different brain regions and in non-synaptic and synaptic mitochondria. Cyclophilin D immunoreactivity was normalized to the VDAC signal. The normalized immunoreactivity is significantly higher in substantia nigra (SNr) when compared to cortex (Cor) and striatum (Str) (p <0.05, n = 4)(A). Non-synaptic mitochondria (NSM) demonstrated significantly higher levels of cypD when compared to synaptic mitochondria (SNM) (p < 0.05, n = 6) (B).