Hence, these genotypes responded equally in terms of inducing caulogenic buds with reference to BA Fig. Biology Plant, 48, Multiple shoots arose on 6-benzylaminopurine BA supplemented Murashige and Skoog media 0.
Reference Micropropagation of Prosopis cineraria L. Approximately 2 g of fresh calli were transferred to a regeneration medium containing different combinations and concentrations of growth regulator and agar as listed in Table 1.
Scientia Agricola Piracicaba, Braz.
Whereas, increased shoot length was recorded on MS medium containing various concentrations of TDZ with 0. Plant Cell, Tissue and Organ Culture, 71, Prosopis cineraria L Druce: Abdus Sattar Quraishi and Salma Quraishi.
Malik A, Kalidhar S. OnLine Journal of Biological Sciences 1 In vitro plant recalcitrance. In the present study, application of 2,4-D alone 0. Generally, callus growth onmedia with both growth regulators showed faster growth and proliferation than those cultured in medium containing 2,4-D alone.
Crop Science Society of America, Inc.
Optimization of callus induction and regeneration system for Pakistani wheat cultivars Kohsar and Khyber The sterilized seeds were germinated on MS medium solidified with 0. Cloning of Maytenus emarginata Willd. Molecular characterization of vernalization response genes in Canadian spring wheat.
We found that apical meristem explants were more responsive than cotyledon leaf explants on all TDZ concentrations Tables 1 and 2.
Embryogenic calli that turned green or yellowish in proliferation medium were transferred to regeneration medium for further development of plantlets. Diversity, Characterization and Utilization.
Seed germination, regeneration and rooting The seeds of cv. Table 2 shows the percentage of callus induction on the surface of the explants after 4 months in culture. As a result she obtained a Masters degree in for her tissue culture research on Solanum tuberosum var.
Conversely, the induction of embryogeneic callus was usually promoted by a relatively higher concentration of 2, 4-D . Electronic Journal of Biotechnology, 12 3:Ozias-Akins, P. () Plant regeneration from immature embryos of peanut.
Plant Cell Rep. 8, – Google Scholar Reinert, J. () Uber die Kontrolle der Morphogenese und die Induktion von Adventivembryonen an Gewebekulturen aus Karotten. In vitro regeneration, a key requisite in the development of transgenic peanut plants is highly genotype dependent.
Differences in the in vitro response among the non Indian genotypes belong to Spanish, Runner, Virginia, and Valencia types had been extensively studied and reported . Regeneration ability of Korean soybean (Glycine max L.) cultivars by in vitro tissue culture.
Department of Life Resources, M.S. Thesis, Sunchon National Univ., Korea. pp. (in Korean). In vitro regeneration of Pakistani peanut (Arachis hypogea L.) varieties using de-embryonated coteledonary explants Farhat Nazir1, Mahmood-ul-Hassan2, Zahid Akram2, Muhammad Matloob Javed2, Shoukat Ali1, Ghulam Muhammad Ali1 and Yusuf Zafar1* 1.
Key words: Fenugreek, in vitro, shoot regeneration, TDZ, IBA_ Introduction Fenugreek (Trigonella foenum-graecum L.) is a legume crop used as a forage, as a green manure and as a source of medicinally important steroid sapogenins (Provorovl et al.
). Twenty-five peanut cultivars from various regions around the world, representing the four market types, namely, Spanish, Valencia, Virginia, and Runner, were evaluated for their potential for in .Download