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. 2005 Jan;206(1):69–78. doi: 10.1111/j.0021-8782.2005.00369.x

Fig. 2.

Fig. 2

Immunofluorescent double-staining with S-100 (red fluorescence) and either NCAM (A), N-cadherin (B) in normal rat sciatic nerve or N-cadherin in the distal stump after axotomy (C) (all adhesion molecules show green fluorescence). NCAM staining in normal nerve sections does not appear to co-localize with S-100, unlike N-cadherin (arrow in B) (orange/yellow staining areas). In the distal stump after axotomy N-cadherin staining co-localizes with S-100 (arrow in C), indicating that Schwann cells may be responsible for the high levels of expression of N-cadherin in distal stumps. Scale bar, 50 µm (objective × 40). NB. Increased exposure times were used for normal nerve sections to allow staining to be adequately visualized.