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  • 1
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 117 (1971), S. 463-475 
    ISSN: 1432-0878
    Keywords: Bone marrow ; Leukocytes ; Electron microscopy ; Histochemistry ; Peroxidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The ultrastructural localization of peroxidase activity has been studied in the cells of normal human bone marrow using the diaminobenzidine peroxidase technique. Peroxidase activity has been localized within the primary (azurophil) granules of the neutrophilic series as well as in the cytoplasmic granules of eosinophils, basophils and monocytes. Peroxidase activity appears within the cisternal system (nuclear envelope, Golgi complex and rough endoplasmic reticulum) of these cells during the period of peroxidase-containing lysosome production. With the cessation of granulogenesis, peroxidase activity disappears from the cisternal system and does not reappear in subsequent developmental stages. In cells incubated in peroxide-free media, staining of granular components, but not of cisternae, is reduced. The inclusion of catalase in peroxide-free media eliminates all staining. This indicates that an endogenous peroxide is present within the cisternae and granules of these cell types.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 170 (1971), S. 81-95 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Buffy coats from blood and bone marrow were fixed in phosphate-buffered glutaraldehyde, exposed to the osmium-zinc iodide (OZI) reagent for 24 hours, dehydrated and embedded in Epon 812. OZI reactivity of blood and bone marrow cells was selectively confined to the cisternae of the rough endoplasmic reticulum (RER), Golgi complex, nuclear envelope and to the mito-chondrial matrices; membranes and other organelles were non-reactive. Some variation in intensity and distribution of OZI reactivity was evident within individual cells and organelles. Continuities between the cisternae of the nuclear envelope and RER as well as between these cisternae and those of the Golgi complex were more conspicuous in OZI preparations than in specimens prepared for routine electron microscopy.The amount and distribution of the cisternal elements and mitochondria within the developing leukocytes and erythrocytes of the bone marrow were evaluated using the OZI technique. All leukocyte granules and their precursor forms fail to stain with the OZI reagent; portions of the Golgi complex most closely associated with the packaging of the cytoplasmic granules also are non-reactive following exposure to the OZI reagent. Reactivity is absent in mature erythrocytes while mitochondria and cisternal components of immature erythroid cells yield positive OZI reactions. Heat, methanol and cyanide inhibit OZI reactivity while a dimorphism of OZI staining is induced between mitochondria and cisternal components by N-ethylmaleimide.
    Type of Medium: Electronic Resource
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