53320 EN embryogenic callus induction from leaf t
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The growth of callus decreased on both dark and light condition at P3 stage of callus proliferation (64 days after transferred from induction medium) (Fig.3).. In contrast
Root arrow as the explant source of 10 days of culture 3.2 Embryogenic callus induction and somatic embryo formation Embryogenic callus induction was conducted on embryogenic callus
Growth regulators which are often used in tissue culture to initiate callus and increase the production of secondary metabolites organogenesis are auxins and cytokinins.. The purpose
The objectives of the present investigation were 1 to improve selected induction culture medium in anther culture of anthurium by 2,4-D application and reduction its strength on callus
The objectives of the present investigation were to improve selected induction culture medium in anther culture of anthurium by 2,4-D application and reduction its strength on callus
The suitable strength of MS Murashige and Skoog nutrient media was determined and the effects of different types of auxins [4-amino-3,5,6-trichloro picolinic acid picloram, 2,4-
Indirect callus formation plant regeneration Excised explants cotyledonary nodes, leaves and shoot tips were aseptically inoculated into prepared MS medium containing callus forming
MS media with 1.5 mg/l 2,4-D and abaxial leaf position can induce callus at 2.4 weeks after planting, caused 100 % percentage of explants forming callus, browning score of 2.1, 10%
