Confocal imaging of MAP2 and GAP43
For immunocytochemistry protocals see: à MAP2/protocals
Link to Confocal intro. "Why use a confocal?"
http://depts.washington.edu/keck/intro.htm
Keck home page.à
http://depts.washington.edu/keck/Leica tutorial on reflectance imaging.
http://depts.washington.edu/keck/mrc600/reflect.htm
GAP43 and MAP2 images were generated in reflectance mode using a Krypton laser at a power setting of 2 (scale = 10) with a 40x objective. The microscope was set up following the instructions found at
http://depts.washington.edu/keck/leica/microscope%20setup.html.