Skip to main content
. Author manuscript; available in PMC: 2022 Oct 14.
Published in final edited form as: J Comp Neurol. 2022 Feb 21;530(10):1658–1699. doi: 10.1002/cne.25307

Figure 9. Combined immunofluorescence labeling for Phox2b, Lmx1b, and FoxP2.

Figure 9.

Immunolabeling for Phox2b (blue, mouse monoclonal antibody) combined with Lmx1b (red) and FoxP2 (green), across six rostral-to-caudal sections through the PB region (a–f), distinguished adult PB neurons from underlying non-PB populations. Additional labeling for TH (magenta) further distinguished Phox2b neurons in the LC from those in the supratrigeminal population. Approximate bregma levels are shown at the bottom-right of each panel. Arrowhead in (a) highlights the KF. Scale bar in (a) is 200 μm and applies to all panels.