Results 151 to 160 of about 863,145 (246)
A Phloxine-Azure-Hematoxylin Sequence for Differential Staining of Cells in Pancreatic Islets
Stain Technology, 1967 Sections of 6 μ from tissues fixed in Susa or in Bouin's fluid (without acetic acid) and embedded in paraffin were attached to slides with Mayer's albumen, dried at 37 C for 12 hr, deparaffinized and hydrated. The sections fixed in Susa were transferred to a I2-K1 solution (1:2:300 ml of water); rinsed in water, decolorized in 5% Na2S2O3; washed in ...
Ricardo Maldonado, Herminia San José
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Staining of Small Lymphoid Nucleoli in Paraffin Sections by Aniline-Azure B
Stain Technology, 1966To see small lymphoid nucleoli clearly in 1-2 μ paraffin sections, the staining of contiguous chromatin masses in the nucleus was suppressed by a hydrolysis-aniline blocking sequence, which produces aldehyde from DNA, and attaches aniline to that aldehyde to make a diphenamine base, thus reducing the acidity of the chromatin and its affinity for basic ...
D. Menzies
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Note from the Biological Stain Commission: Revision of Azure B Assay Protocol
Stain Technology, 1988 (1988). Note from the Biological Stain Commission: Revision of Azure B Assay Protocol. Stain Technology: Vol. 63, No. 1, pp. 65-68.
Eric A. Schenk, Elmer Stotz
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Stability of azure B–eosin Y staining solutions
British Journal of Haematology, 1985 Summary. The stability of azure B–eosin Y staining solutions of varying composition and of a routine May Grunwald Giemsa (MGG) stain were studied by analysis of the density histogram of white blood cells obtained by an image analysis computer. The stability appeared to be variable and depended on the concentration of the dyes, the molarity of the ...
M. Bins, W. Huiges, M. R. Halie
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Biotechnic & Histochemistry, 1996 Transverse paraffin sections of mature greenwood stems of rose (Rosa x hybrida) and flowering dogwood (Cornus florida L.) were stained with Bismarck brown followed by azure B or toluidine blue 0. The Bismarck brown was replaced by thiazin dye metachromasia in all structures except the cuticle which remained brown or yellow.
Effin T. Graham, Priyavadan A. Joshi
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A Simple Methylene Blue-Azure Ii-Basic Fuchsin Stain for Epoxy-Embedded Tissue Sections
Stain Technology, 1974 One micron-thick sections of tissues fixed in glutaraldehyde, or in glutaraldehyde followed by osmium tetroxide, and embedded in a variety of plastic resins were stained in a methylene blue-azure II solution at 65 C, then counterstained in 0.05% basic fuchsin in 2.5% ethanol at room temperature (24 C). Considerable variation was found in methylene blue-
Charles D. Humphrey, Fred E. Pittman
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Effect of malononitrile dimer on RNA concentration of neurons as demonstrated by azure B staining
Cells Tissues Organs, 1976 Malononitrile dimer was administered to mice by single or by chronic (40 day) injections. The concentration of RNA in neurons of the brain was determined on histological sections by means of azure B staining. The nucleolus and Nissl substance of the several types of large neurons studied had a significantly higher concentration of RNA in the drug ...
Kuldip Singh Dhindsa +1 more
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Sulfation-Hematoxylin-Azure B as an Alternative to Periodic Acid-Schiff Staining
Laboratory Medicine, 1989 Gentle sulfation of formalin-fixed tissue sections followed by staining in a hematoxylin-azure B sequence results in bright blue staining of tissue elements that stain with the periodic acid-Schiff reaction—especially basement membranes. The stain is relatively rapid, simple, and permanent, is performed with inexpensive, readily available laboratory ...
Stanley H. Shapiro
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The Staining of Moist Preparations with Azure-eosin (Giemsa)
The American Journal of the Medical Sciences, 1910 &NA;
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Methylene blue/azure II staining solution
Cold Spring Harbor Protocols, 2010 openalex +2 more sources