Regenerated plant in-vitro culture method for Sirindhorn michelia figo
A technology for in vitro culture and regeneration of plants, applied in the field of biological in vitro tissue culture seedlings, can solve the problems of hindering the development of reproductive technology, browning, high pollution rate, etc., achieve high induction rate and survival rate, low transplant survival rate, precious, The effect is simple and feasible
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Embodiment 1
[0033] Example 1 The following steps are used to achieve the in vitro culture regeneration of Sirindhorn Michelle:
[0034] (1) Treatment of explants and their materials: In the Shenzhou Mulan Garden in Xuwen County, Guangdong Province, the young shoots that germinated on the main pole of the 7-year-old Sirindhorn Michelle, which is healthy and free of diseases and insect pests, were taken after on-site fresh-keeping treatment , brought back to the laboratory at low temperature; cut off the leaves on the tender shoots in the laboratory, rinse with running water after cleaning with bromogeramine, and cut into 2 cm stem segments with 1-2 axillary buds;
[0035] (2) Establish sterile propagules: sterilize the pruned stems in the laboratory with 0.1% mercuric chloride for 3 minutes, then wash 4 times with sterile water, and inoculate a section of a bottle on the primary medium MS1 , cultured for 15 days at room temperature of 30°C, 8 hours of light per day, and light intensity of ...
Embodiment 2
[0045] Example 2 The following steps are used to realize the regenerated plants of Sirindhorn Michelle in vitro:
[0046] (1) Treatment of explants and their materials: In the Shenzhou Mulan Garden in Xuwen County, Guangdong Province, the young shoots that germinated on the main pole of the 7-year-old Sirindhorn Michelle, which is healthy and free of diseases and insect pests, were taken after on-site fresh-keeping treatment , brought back to the laboratory at low temperature; cut off the leaves on the tender shoots in the laboratory, rinse with running water after cleaning with bromogeramine, and cut into 2 cm stem segments with 1-2 axillary buds;
[0047] (2) Establish sterile propagules: sterilize the pruned stems in the laboratory with 0.1% mercuric chloride for 10 minutes, then wash with sterile water for 3 times, and inoculate a section of a bottle on the primary medium MS1 , cultured for 20 days at room temperature of 20°C, 12 hours of light per day, and light intensity...
Embodiment 3
[0057] Embodiment 3 adopts the following steps to realize the in vitro culture regeneration plant of Sirindhorn Michelle:
[0058] (1) Treatment of explants and their materials: In the Shenzhou Mulan Garden in Xuwen County, Guangdong Province, the young shoots that germinated on the main pole of the 7-year-old Sirindhorn Michelle, which is healthy and free of diseases and insect pests, were taken after on-site fresh-keeping treatment , brought back to the laboratory at low temperature; cut off the leaves on the tender shoots in the laboratory, rinse with running water after cleaning with bromogeramine, and cut into 2 cm stem segments with 1-2 axillary buds;
[0059] (2) To establish sterile propagules: sterilize the pruned stem segments with 0.1% mercuric chloride for 5 minutes in the laboratory, then wash with sterile water for 3 times, and inoculate a section of a bottle on the primary medium MS1 , cultured for 30 days at room temperature of 26°C, 10 hours of light per day, ...
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