Monday, February 25, 2019

Fixation and Fixatives

ALCIAN BLUE RATIONALE FOR USE Alcian amobarbital sodium is a water soluble, amphoteric copper phthalocyanine, which is most often use as a basic tinge. In general, alcian glooming has an affinity for sulfated and carboxylated groups of venereal disease mucopolysaccharides, but the specialised group demo is dependent on the blot solution pH. RECOMMENDED FIXATIVES 10% neutral buffered formalin and Bouins fixative. AVOID Chromate Fixatives mode OF ACTION (1, 2, 3) Alcian easy binds electrostatically with the acidic groups in the mucopolysaccharide molecule.The components to be demonstrated be intensely stained if the dyer solution is used at the specific pH at which the reactive groups are copiousy ionized. To achieve full ionization of the reactive groups, some alcian blue methods begin with a rinse of sections in the appropriate pH solution prior to dye with the dye solution. In general, strongly sulfated mucins react more consistently at humble pH levels. Above a pH of 1. 0 their reactions are variable. At a pH of 0. 2 only strongly sulfated mucosubstances will be demonstrated, while weak sulfated mucins stain well between a pH of 1. 0 2. 5, and often below 1. . Carboxylated mucins react with alcian blue at pH 2. 5. Alcian blue produces an intense greenish-blue or teal coloration. To ensure this colour is not lost during subsequent chemical and dye treatments, such as those put up in the Alcian Blue-Verhoeffs van Gieson procedure and Movats Pentachrome, alcian blue is converted to an insoluble pigment. By exposing alcian blue stained sections to a pre-heated 80C alkaline alcohol solution, alcian blue is converted to the insoluble pigment, monastral fast blue. hike up exposure of the sections to various decolorizers and dyes, fails to change the alcian blue intensity.QUALITY CONTROL AND CONTROL MATERIALS 1. captivate control tissue papers include colon and small intestine. If lung sections contain bronchi with mucous glands, are used as a con trol, the tech should be aware that gristle matrix will also stain at approximately pH 2. 5. 2. To avoid coloration of hyaluronic acid found in connective tissue matrix or amorphous ground substance, the tissue section hind end first be treated with a solution of testicular streptococcal hyaluronidase before staining with alcian blue. Testicular hyaluronidase requires only 2 hours of incubation versus 24 hours with streptococcal hyaluronidase. . Alcian blue powder solubility whitethorn decrease after storage of more than triad years, but heartfelt staining results have been reported with dye lots older than three years (4). 4. The dye solution pH is critical to ensure notification of specific chemical groups. pH 0. 2 -only strongly sulfated mucins demonstrated pH1. 0 -strongly and weakly sulfated mucins pH 2. 5 -carboxylated and weakly sulfated mucins 5. To ensure the quality of staining at the appropriate pH, the section may be rinsed in the root solution prior to staining in the dye, i. e. , rinsing in pH 2. , 3% aqueous acetic acid solution prior to placing the sections in the pH 2. 5 alcian blue solution, which is prepared by combining alcian blue dye powder in a 3% aqueous acetic acid solution. 6. Some procedures indicate it is important to avoid rinsing the stained slides in water after treatment in alcian blue dye. Blotting the slides dry after staining is recommended. 7. It is important to avoid celloidinization of tissue sections because alcian blue has a strong affinity for celloidin. 8. A white haze may come on on the keep going of the glass slide after staining with thermonuclear fast red and contact with the air.Moistening a kimwipe or facial tissue with saliva and rubbing the back of the glass will have the haze. keep this with cleaning of the glass using a kimwipe moistened with 100% ethanol to remove the saliva. 9. Cut paraffin sections at 4-6 microns. REFERENCES 1. Bancroft J. D. and Stevens A. Theory and Practice of Histological T echniques, second edition. Churchhill Livingstone, 1982. 2. Kiernan J. A. Histological and Histochemical Methods Theory and Practice, Pergamon Press, 1981. 3. Sheehan D. C. and Hrapchak B. B. Theory and Practice of Histotechnology, second edition, C.V. Mosby Co. , 1980. 4. Shrenk E. occupation from the biological Stain Commission-a newly certified dye-Alcian blue 8GX. Stain. Tech. 56(3), 129, 1981. ALCIAN BLUE pH 2. 5 SOLUTIONS a. 1% Alcian Blue Solution pH 2. 5 Alcian Blue 8GX (C. I. 74240)1gm 3% Glacial acetic acid100ml (3 ml. glacial acetic acid to 97 ml. distilled water) leave a crystal of thymol to prevent mold growth. The solution buttocks be filtered and reused. b. Nuclear Fast Red (Kernechtrot) Solution (pg. 19) PROCEDURES (1, 2) 1. Deparaffinize and hydrate slides to distilled water. (See Note 1) 2.Stain in alcian blue solution for 30 minutes. Filter solution back for reuse. (See Note 2) 3. Wash for 2 minutes in running criticize water. 4. wash away in distilled wa ter. 5. Counterstain in nuclear fast red for 3 to 5 minutes. Quickly transfer slides to distilled water. Filter solution back for reuse. 6. Rinse slides in distilled water. 7. Dehydrate, clear, and mount. If a cloudy haze appears on the side mean to quality control information, 8. COLOR RESULTS Carboxylated and weakly sulfated acid mucins light blue to medium greenish blue Nuclei-reddish pink.NOTE 1. After dance step 1, the slides may be placed in a pH 2. 5, 3% aqueous acetic solution for 1 minute, then proceed to step 2. 2. After step 2, the slides can be blotted dry, instead of rinsing in running rap water and distilled water. Continue the procedure with step 5. REFERENCES 1. Lev R. and Spicer S. S. Specific staining of sulfate groups, with Alcian blue at low pH. J. Histochem. Cytochem. , 12309, 1964. 2. Sheenhan D. C. and Hrapchak B. B. Theory and Practice of Histotechnology, 2nd edition. C. V. Mosby Co. , 1980

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