Figure 1. Runx2 gene and protein expression is detectable in neurons of the adult mouse brain.
A) Qualitative PCR analysis of Runx2 mRNA (289 bp) expression in the suprachiasmatic nucleus (SCN) of adult mice. Lane 1: 100 bp molecular weight standard ladder (black arrowhead: 300 bp; grey arrowhead: 500 bp). Lane 2–4: Runx2 (289 bp) PCR product from reactions performed using E15 mouse calvarial bone mRNA extracts and Runx2-specific primers. Lane 5–7: Runx2 (289 bp) PCR product from reactions performed using adult mouse SCN mRNA extracts and Runx2-specific primers. Sequencing confirmed the identity of all positive PCR amplification products. B) Western blot analysis of Runx2 protein (∼60 kDa; black arrowhead) expression in the SCN of adult mice. Lane 1: Molecular weight standard ladder. Lane 2–3: protein isolated from E15 mouse calvarial bone. Lane 4–5: protein isolated from SCN of adult mice. GAPDH (∼37 kDa; grey arrowhead) protein detection served as a loading control. C) Immunolabelling of Runx2 (green) and NeuN (red) in the frontal cortex. Overlay image showing co-localization of Runx2 and NeuN (yellow). Scale bar: 50 µm.
