Under the stain, myelin fibers appear blue, neuropil appears pink, and nerve cells appear purple. Tissues sections are treated over an extended period of time (usually overnight) and then differentiated with a lithium carbonate solution.[4]
Combination methods
The combination of LFB with a variety of common staining methods provides the most useful and reliable method for the demonstration of pathological processes in the CNS.[2] It is often combined with H&E stain (hematoxylin and eosin), which is abbreviated H-E-LFB, H&E-LFB. Other common staining methods include the periodic acid-Schiff, Oil Red O, phosphotungstic acid, and Holmes silver nitrate method.[2]
^Kluver H., Barrera E. (1953). "A method for the combined staining of cells and fibers in the Nervous system". J. Neuropathol. Exp. Neurol. 12 (4): 400–403. doi:10.1097/00005072-195312040-00008. PMID13097193.