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  • 1
    ISSN: 1573-5028
    Keywords: direct gene transfer ; gene rearrangements ; Nicotiana tabacum ; particle gun ; transformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transgenic tobacco plants and progeny carrying coding sequences for neomycin phosphotransferase II (NPTII) and beta-glucuronidase (GUS) were recovered following microprojectile bombardment of tobacco leaves. Transgenic plants were regenerated from bombarded leaf pieces of tobacco cvs. ‘Xanthi’ and ‘Ky 17’ which were cultured in the presence of 100 or 200 μg/ml kanamycin for six to eight weeks. Among 160 putative transgenic plants from at least 16 independent transformation events 76% expressed NPTII, and 50% expressed GUS. Southern analysis of plants expressing either one or both of the enzymes indicated DNA in high molecular weight DNA in 8 of 9 independent transformants analyzed. Two independent transformants and their progeny were analyzed in detail. Analysis of progeny for quantitative enzyme levels of NPTII and GUS, and Southern analysis of parents and progeny clearly demonstrated that the genes were transmitted to progeny. One transformant demonstrated Mendelian ratios for seed germination on kanamycin-containing medium while the other transformant had non-Mendelian ratios. DNA analysis of progeny indicate complex integration of the plasmid DNA, and suggest that rearrangements of this DNA has occurred. These results are consistent with other methods of direct DNA uptake into cells, and verify that the microprojectile bombardment method is capable of DNA delivery into intact plant cells which can give rise to transgenic plants and progeny.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0603
    Keywords: Co-culture ; Cell culture inserts ; Rinsing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A goal of our laboaatory is to define putative intercellular communication mechanisms between myofibers and adipocytes. In pursuit of this objective we established a co-culture system incorporating commercially available microporous cell culture inserts. These cell culture inserts provide separation of cells bathed in a common media environment. Isolation and evaluation of the conditioned media from such systems allows detection of autocrine or paracrine agent production by either cell type. However, the process of rinsing cells plated on inserts prior to initiating co-culture may damage insert integrity and may dilute (added) defined treatment medium by introducing residual rinse medium. We have developed a method to rinse microporous membrane inserts before the addition of defined treatment medium. This rinsing technique decreases damage to inserts and reduces the volume of residual medium on all physical aspects of the insert.
    Type of Medium: Electronic Resource
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