Cytokinins and coconut water promoted abnormalities in zygotic embryo culture of oil palm

No axillary shoot induction was observed from the explants with no cytokinin pretreatment (control, MS culture medium free of plant growth regulators).. In addition, no

After six months of culture, the adventitious shoots obtained from Experiment I and II were transferred to K medium and MS medium, respectively, containing 0.2 mg/L NAA, 2%

Shoot apex in induction medium; (b) primary somatic embryos at the globular stage on the explant surface after ten days of culture in induction medium; (c) torpedo

In order to stimulate shoot elongation and proliferation, calli with short adventitious buds were first transferred to half-strength MS medium supplemented with

(a) Inoculation of shoot tip in initial culture medium supplemented with 5 mg l -1 BA and 0.1 mg l -1 IAA (b) multiple shoot formation on shoot apices in MS medium supplemented

To initiate the callus induction and shoot regeneration from the axenic leaf and internode tissues, in vitro -regenerated shoots maintained for nearly six months

Table 1 - Effect of plant growth regulators on shoot regeneration from shoot tip explants of Cassia angustifolia in MS medium after four weeks of culture.. Addition of the IAA

BAP and TDZ) (A) and type of cytokinin (BA, BAP and TDZ) at different inoculation times (30, 60 and 90 days) (B); shoot length (C) and formation of lateral shoots (D) formed in