Rapid tissue culture propagation method for miscanthus floridulu somatic embryo of mscanthus plant
A plant and awn body technology, which is applied in the field of tissue culture and rapid propagation of Miscanthus penicillium somatic embryos, can solve the problems of different healing rate and differentiation rate, failure to obtain embryogenicity, and failure to obtain embryogenicity, etc., to achieve healing The effect of high wound reproduction rate, high value-added rate and stable value-added
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[0025] A method for rapid propagation of somatic embryo tissue culture of Miscanth acanthus, the steps of which are:
[0026] 1. Selection of young panicles: Select young panicles that are in the formation stage of Yinghua primordium. The seeds in the young panicles have not yet formed, the central axis is relatively soft, and the basic branches have not yet formed.
[0027] 2. Use the primary culture medium for primary induction: cut it into 2-3 cm pieces, first sterilize it with 75% alcohol for 30 seconds, then soak it in 0.1% mercury chloride for 5 minutes, then rinse it with sterile water three times, and inoculate it On the primary induction medium of young panicles. After 35 days of primary induction, embryogenic callus was obtained. The culture conditions are 25°C, 16 hours of light per day, and the light intensity is 2000LX. The primary induction medium is: A: MS medium supplemented with kinetin KT1-5mg / L, naphthaleneacetic acid NAA0.1-0.5mg / L, sucrose 30g / L, Phytage...
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