Alkaline Phosphatase for Glycol Methacrylate Sections
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- Procedure:
- Incubate sections in the incubating medium at room temperature for 1 - 3 hours. Two hours is sufficient in most cases.
- Wash in distilled water for 2 minutes.
- Counterstain with Nuclear Fast Red for 5 - 10 minutes.
- Wash in distilled water for 2 minutes.
- Air dry and coverslip.
- Results:
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- Nuclei - red
Sites of enzyme activity - blue
To preserve the reaction product, selection of the right mounting (coverslipping) medium is important. -
- Solutions:
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- Incubating Medium
- Naphtol AS-MX phosphate, di-sodium salt (Sigma) - 5 mg
- N,N - dimethylformamide - 0.25 ml
- Fast Blue BB (Sigma) - 30 mg
- Distilled Water - 25 ml
- Buffer Solution - 25 ml
- 10% Magnesium Sulfate Solution. - 2 drops
- Prepare fresh, shake well and filter before use.
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- Buffer Solution
- 0.2M Tris (hydroxymethyl)-aminomethane - 2.4 gm
- Distilled water - 100 ml
- Adjust the pH of the buffer to 8.9 with dilute HCl and store at 4°C.
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- Nuclear Fast Red
- To 0.2 gm of Nuclear Fast Red add 200 ml of boiling 0.5% aluminum sulfate solution.
- Keep boiling for 5 - 10 minutes
- Allow to cool and filter before use.
- Citation:
Gerrits, P. O. and Smid, L., "Staining Procedures for Tissues Embedded in 2-Hydroxyethyl Methacrylate", Heraeus Kulzer.
Additional Online Resources
Technovit Glycol Methacrylate Embedding Kits
Plastic Embedded Tissue: More Techniques and Protocols
Light Microscopy Supplies
Energy Beam Sciences, Inc. 11 Bowles Road · Agawam, Massachusetts 01001-2925
Phone: 800-992-9037 or 413-786-9322 · Fax: 413-789-2786
E-mail:
ebs@ebsciences.com
