ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 52 (1998), S. 209-212 
    ISSN: 1573-5044
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In vitro shoot organogenesis of peppermint and spearmint was obtained from leaf disks. Regeneration occurred within six weeks of placement in culture. Best results were obtained when explants were cultured for two weeks onto Murashige and Skoog medium supplemented with 300 mM mannitol, 2.0 μM 6-benzyladenine and 2.0 μM indole-3-butyric acid, and then transferred on a medium without mannitol and containing 0.5 μM α-naphthaleneacetic acid, 9.0 μM 6-benzyladenine and 0.5 μM thidiazuron. Using these culture conditions, percentages of regeneration were 78% for peppermint and 49% for spearmint. Because of its efficiency, this leaf disk regeneration method could be a suitable tool for genetic transformation with Agrobacterium tumefaciens.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 57 (1999), S. 75-78 
    ISSN: 1573-5044
    Keywords: Agrobacterium tumefaciens ; genetic transformation ; GUS ; Mentha spicata ; Mentha arvensis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The stable integration of GUS and NPTII genes in Mentha arvensis and M. spicata has been achieved by Agrobacterium tumefaciens-mediated gene transfer. Transformation assays were performed by cocultivating plant leaf disks with either GV2260/GI or EHA105/MOG Agrobacterium strains. Transgenic plants were selected on medium containing 150 mg l−1 kanamycin. Transgene presence and structure was studied by the use of PCR analysis and Southern blot hybridization. Transgene expression was evaluated by RT-PCR and transgene product activity by a histoenzymatic GUS assay.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...