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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 169 (1976), S. 277-287 
    ISSN: 1432-0878
    Keywords: Rabbit gametes ; Cryofractography ; Scanning electron microscopy ; Transmission electron microscopy ; Zona pellucida
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Rabbit ova fertilized in vitro were prepared for scanning electron microscopy by ethanol-cryofracturing and critical-point drying methods and were also embedded and sectioned for transmission electron microscopy. Study of a region of interaction between sperm and zona pellucida with scanning electron microscopy reveals the latter to be composed of a complex network of fibers interspersed with numerous pores. Transmission electron microscopy of the same region reveals a “typical” homogeneous composition of the zona pellucida. Ultrastructural observations of thin sections passing through the region of sperm-egg interactions or through other regions of the ovum or its investments reveals very little methodological distortion of the various intracellular organelles or matrix. Application of the procedures described provides not only an elucidation of surface detail but also reveals intracellular cytoplasmic information about the same specimen during in vitro fertilization.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 8 (1983), S. 183-197 
    ISSN: 0148-7280
    Keywords: acrosin ; proflavin-sepharose ; anti-acrosin antibodies ; rabbit ; fertilization inhibition ; immunoreproduction ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Rabbit acrosin was purified from detergent extract of epididymal spermatozoa by molecular-sieve Chormatography (Sephadex G-75) and Priflavin-Sepharose affinity chromatography. Affinity Purified rabbit acrosin (Specific activity = 63.7 U Per mg Protein) exhibited one major band (Mr = 36,000) on SDS-polyacrylamide-slab gel electrophoresis. Sheep werweantibodies, Preared against acid-glycerol-stabilized acrosin, were Fractionated sequentitally with 50 and 33% ammonium sulfate. Anti-acrosin immunoglobulins were specific for the acrosome as evidenced by indirect fluorescence lebeling, and they inhibited acrosin's proteolytic activity when essayed for their effect on fertilization invivo, antiacrosin-treated sperm produced the lowest persent fertility (7.1%) followed by preimmune y-globulins(69%), Krebs-ringer hosphate-glucose-serum(96.4%) Analysis of antibody-treated sperm revealed no significiant chang in their motility or agglutination patterns. Antiacrosin antibodies, therefore, can effectivily neutrlize acrosin and inhibit fertilization when placed at the site of sperm-egg interaction in vivo.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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