Zobrazeno 1 - 7
of 7
pro vyhledávání: '"A. H. McKently"'
Publikováno v:
Ecological Restoration. 18:249-253
Autor:
A. H. McKently
Publikováno v:
Plant Cell, Tissue and Organ Culture. 42:251-254
Genotypes representing the three botanical varieties of peanut (Arachis hypogaea L.) were assessed for somatic embryogenesis and subsequent plant conversion from mature zygotic embryo axes. Explants were initially cultured on Murashige and Skoog medi
Autor:
A. H. McKently
Publikováno v:
In Vitro Cellular & Developmental Biology - Plant. 27:197-200
Plant regeneration via somatic embryogenesis was obtained in peanut (Arachis hypogaea L.) from axes of mature zygotic embryos. The area of greatest embryogenic activity was a 2-mm region adjacent to and encircling the epicotyl. Somatic embryogenesis
Publikováno v:
Crop Science. 30:192-196
(...) This study was designed to assess the regeneration response of explants taken from the seed of peanut (Arachis hypogaea L.). Complete plants were regenerated from in vitro-cultured embryo axes and embryonated and deembryonated cotyledons that w
Autor:
A. H. McKently
Publikováno v:
Somatic Embryogenesis and Synthetic Seed II ISBN: 9783642786457
Arachis hypogaea L., the cultivated peanut, also called groundnut, is an important source of oil and protein and makes a major contribution to human nutrition. Peanut is native to South America with its primary center of origin believed to occur in s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a5325508c49ab1ddaeba44d1f555794
https://doi.org/10.1007/978-3-642-78643-3_18
https://doi.org/10.1007/978-3-642-78643-3_18
Publikováno v:
Plant cell reports. 14(11)
Transgenic peanut (Arachis hypogaea L.) plants have been produced using an Agrobacterium-mediated transformation system. Zygotic embryo axes from mature seed were cocultured with Agrobacterium tumefaciens strain EHA101 harboring a binary vector that
Autor:
Alexandra H. McKently, James B. Adams
Publikováno v:
HortScience. 29:921
•s ‐1 photoperiod provided by cool-white fluorescent lamps and evaluated for axillary shoot multiplication 45 days after culture initiation. Data were subjected to an analysis of variance. Within 30 days of culture initiation, callus and multiple