EMS26312
Components:
Coleman's Feulgen
Light Green Stock Solution 0.2%
Periodic Acid 0.5% Aqueous
Acid-Alcohol 1%
Ammonia Water 0.3%
Schiff'S Reagent
Light Green Working Solution
Harris Haematoxylin
Fixation:
10% Buffered Neutral Formalin or Zenker’s
Sections:
Cut Paraffin, 6µm
Staining Procedures:
- Deparaffinise and hydrate to distilled water.
- Oxidise in Periodic Acid, 0.5%, 5 minutes and rinse in distilled water.
- Stain in Coleman’s Feulgen or Schiff’s Reagent, 15 minutes and wash in running water to develop the pink colour, 10 minutes.
- Counterstain in Harris Hematoxylin 6 minutes, or Light Green Working Solution 5 – 10 seconds. Light Green is better used when delineation of fungi is required. Prepare the working solution by diluting Light Green, 0.2% Solution 1:5 ratio with distilled water; proceed to step #7, dehydration. Tap water and ammonia decolourise Light Green.
- Wash in running water and transfer to Acid Alcohol, 1%, for 3 -10 quick dips. Wash again in distilled water.
- Dip in dilute Ammonia Water, 0.3%, to blue the sections and again wash in running water for ten minutes.
- Dehydrate in 95% alcohol, absolute alcohol, and clear in xylene, two changes each.
- Mount with Permount or DPX.
Stain Results:
Nuclei | Blue |
Fungi | Red |
Background, when Light Green is used as the counterstain | Green, pale |
References:
McManus, JFA: Stain Tech.; 23:99 (1948).
AFIP, Manual of Histologic Staining Techniques; L.G. Luna, 3rd edition, New York: McGraw-Hill Publication, c. 1968, p. 160.
Mowry, R.W.: Annals of the New York Academy of Science; 106: 402 (1963).
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