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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Company
    Nature biotechnology 6 (1988), S. 1035-1040 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] The successful expression of foreign genes in model systems such as tobacco and tomato highlights the enormous potential of the marriage of molecular biology and plant cell culture. But biological and technical problems still hamper the application of these technologies to important food crops such ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 278 (1979), S. 51-54 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. l Growth kinetics in response to illumination and darkness, a, Blue-light inhibition and recovery: blue light was provided by an opposed pair of collimators (to prevent phototropism) focused on the 5-mm region of the hypocotyl measured -10 mm from the cotyledonary node. The light source ...
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-994X
    Keywords: plant viral promoter ; caulimovirus ; strawberry vein banding virus ; zucchini yellow mosaic virus ; particle bombardment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A putative promoter from the strawberry vein banding caulimovirus (SVBV) genome was identified by its ability to drive infection with full-length cDNA of the zucchini yellow mosaic RNA potyvirus (ZYMV). A high rate of infection was obtained with the cDNA under control of the SVBV promoter using particle bombardment technology. The SVBV promoter shows 60% homology to the cauliflower mosaic virus 35S promoter in the domain spanning the conserved motifs of CCACT (at −83) and the TATA box (at −31), to the transcription start. The 3′-end one-third of the putative promoter (328 bp) was sufficient to invoke full infectivity with the ZYMV clone, and drove transient reporter gene expression in Solanaceae and Cucurbitaceae transformed with a binary plant transformation vector. Stable expression of a reporter gene (GUS) under control of the truncated SVBV promoter was shown in transformed tobacco shoots in roots, leaves and stems.
    Type of Medium: Electronic Resource
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