Results 91 to 100 of about 1,285 (142)

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 ...
BINS, M, HUIGES, W, HALIE, MR
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Azure B Bromide Staining of Regenerating Muscle

American Journal of Clinical Pathology, 1966
Paraffin sections of regenerating muscle fibers color intensely blue or purple with the metachromatic stain azure B bromide. These darkly stained fibers show excellent cellular detail in cytoplasm as well as nuclei. They contrast conspicuously with the pale blue of adjacent normal muscle. Differential staining of nucleic acids is the principle on which
Fae D. Wood, Carl M. Pearson
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Which granules can be stained with azure B and eosin?

Blood cells, 1990
The standardized stain composed of pure azure B and eosin, as published by Wittekind and colleagues in 1986, demonstrated granules in neutrophilic leucocytes that were much coarser than those seen after staining with conventional Romanowsky-Giemsa methods. These granules belong to at least two classes.
H, Kurz, G, Leder, O, Leder
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An Improved Formulation of Nocht's Azure-Eosin Stain for Plastic Embedded Material

Stain Technology, 1983
The popular azure-eosin stain of Nocht has been reformulated to provide consistent, intense staining of semithin sections of water-miscible methacrylate embedded tissues.
R M, Franklin, M T, Martin
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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 ...
R, Maldonado, H, San José
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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 H. Stotz
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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 ...
K S, Dhindsa, H E, Enesco
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Azure B-Eosin APAAP Staining: a Method for Simultaneous Hematological and Immunological Cell Analysis

Biotechnic & Histochemistry, 1995
Azure B-eosin APAAP staining allows simultaneous analysis of peripheral blood and bone marrow cells for hematological characteristics and immunological cell marker profiles. A defined sequence of staining procedures maintains characteristic components of the Romanowsky-Giemsa stain whereas cell antigens can be detected immunologically using the ...
B, Koch, B, Eberhardt, M, Westerhausen
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Staining of Small Lymphoid Nucleoli in Paraffin Sections by Aniline-Azure B

Stain Technology, 1966
To 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 ...
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Quantification and Characterization of Glycosaminoglycans at the Nanogram Level by a Combined Azure A-Silver Staining in Agarose Gels

Analytical Biochemistry, 1994
A rapid, sensitive, and nonradioactive method has been developed for the quantification and characterization of glycosaminoglycans. The method is based on the separation of different types of glycosaminoglycans in agarose gel and subsequent fixation and staining with the cationic dye azure A, followed by silver enhancement.
C H, van de Lest, E M, Versteeg, J H, Veerkamp, T H, van Kuppevelt   +3 more
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