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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of assisted reproduction and genetics 15 (1998), S. 154-157 
    ISSN: 1573-7330
    Keywords: intracytoplasmic injection ; mouse ; ROSI ; ROSNI ; spermatid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose: This study investigated whether K + -rich medium is better than pure NaCl solution or Na + -rich cell culture medium for handling round spermatid nuclei prior to injection into oocytes (ROSNI). Methods: Round spermatids of the mouse were isolated and stored in isotonic NaCl, a cell culture medium (CZB), or a nucleus isolation medium (NIM) before injection into oocytes. The rates of normal fertilization, embryonic development in vitro, and birth of normal offspring after transfer of embryos to foster mothers were determined. Results: In vitro development of ROSNI-produced zygotes to blastocysts was the same when “naked” spermatid nuclei were exposed briefly to three media. However, a long (60-min) exposure of the nuclei to NA + -rich medium was detrimental. In K + -rich NIM “naked” spermatid nuclei best retained their ability to participate in normal embryonic development. Conclusion: NIM was better than Na + -rich medium for retaining isolated spermatids competent to participate in normal embryonic development.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7330
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of assisted reproduction and genetics 11 (1994), S. 367-372 
    ISSN: 1573-7330
    Keywords: coculture ; cryopreservation ; human oviduct epithelial cell ; blastocyst ; mouse embryo
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose The effect of coculturing mouse embryos with cryopreserved human oviduct epithelial cells was investigated. The cryopreserved cells in Cellbanker were thawed and cultured in Richard D. Goldsby culture medium to establish monolayers. Two-cell-stage mouse embryos were cultured alone (control group) or cocultured with monolayers established from cryopreserved cells (cryopreserved coculture group) or from fresh cells (fresh coculture group). The rates of embryo development and the qualities of the blastocysts in the three groups were compared. Results The two coculture groups had significantly higher blastocyst development rates (cryopreserved coculture group, 81.6%; fresh coculture group, 82.2%) than the control group (63.1%). The two coculture groups had significantly more blastomeres (cryopreserved coculture group, 108.3 ± 25.9; fresh coculture group, 108.4 ± 25.1) than the control group (87.7 ± 31.9). Conclusion The method of cryopreservation of human oviduct epithelial cells using Cellbanker is simpler than conventional cryopreservation methods. These cryopreserved human oviduct epithelial cells may provide a constant supply of cells for coculture for in vitro fertilization and embryo transfer.
    Type of Medium: Electronic Resource
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