Abstract
Neurons and glia can be labeled using fluorescence immunocytochemistry, fluorescent tract-tracers, and a variety of other techniques that use fluorescence. Combining these methods to label tissue with two or more fluorescent probes can increase the power of an experimental design. The present paper examines the issues related to the use of laser-scanning confocal microscopy to image combinations of fluorescent labels and recommends specific combinations of lasers, filters, and fluorophores.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 121-140 |
| Number of pages | 20 |
| Journal | Neuroprotocols |
| Volume | 2 |
| Issue number | 2 |
| DOIs | |
| State | Published - Apr 1993 |