Method for Obtaining Regenerated Plants from Cedar Stem Tissue Culture
A technology for tissue culture and regeneration of plants, applied in botany equipment and methods, plant regeneration, horticultural methods, etc., can solve problems such as danger, insufficient supply of high-quality seedlings, and low seed yield, so as to maintain good traits and promote healthy and rapid growth The effect of development
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Embodiment 1
[0026] (1) Take the stem material, soak it in detergent solution for 30 minutes, gently brush off the surface dust with a brush, and cut it into independent small branches with terminal buds, the length is 5cm, put the branches in a beaker, and rinse with running water 3h, dry the water, then soak in 0.2% carbendazim solution for 33min, wash twice with distilled water, put it in a sterile culture room for aseptic disinfection, and use 75% alcohol under the ultra-clean workbench After disinfection for 15 seconds, soak in 0.1% mercuric chloride for 7 minutes, then wash with sterile water for 5 times, and blot dry with sterile gauze for later use;
[0027] (2) Induction culture, cut off the 2.5cm stem segment, cut off 2 / 3 of the needle length, and insert it into the induction medium (the induction medium is WPM basic medium + 6-BA1.0mg.L -1 +IBA0.03mg.L -1 + 30g.L sucrose -1 +Agar 7g.L -1 ), cultured in a dark incubator for 100 hours, and then placed in a light incubator for c...
Embodiment 2
[0032] (1) Take the stem material, soak it in detergent solution for 25 minutes, gently brush off the surface dust with a brush, and cut it into independent small branches with terminal buds, the length is 5cm, put the branches in a beaker, and rinse with running water 3h, dry the water, soak in 0.2% carbendazim solution for 30min, wash twice with distilled water, put it in a sterile culture room for aseptic disinfection, and use 75% alcohol under the ultra-clean workbench After disinfection for 10 seconds, soak in 0.1% mercuric chloride for 6 minutes, then wash with sterile water for 4 times, and blot dry with sterile gauze for later use;
[0033] (2) Induction culture, cut off 2cm stem segments, cut off 2 / 3 of the needle length, and insert induction medium (induction medium is WPM basic medium + 6-BA0.8mg.L -1 +IBA0.05mg.L -1 + 30g.L sucrose -1 +Agar 7g.L -1 ), cultured in a dark incubator for 72 hours, and then placed in a light incubator, and the buds began to swell and...
Embodiment 3
[0038] (1) Take the stem material, soak it in detergent solution for 25 minutes, gently brush off the surface dust with a brush, and cut it into independent small branches with terminal buds, the length is 5cm, put the branches in a beaker, and rinse with running water 3h, dry the water, soak in 0.2% carbendazim solution for 30min, wash twice with distilled water, put it in a sterile culture room for aseptic disinfection, and use 75% alcohol under the ultra-clean workbench After disinfection for 10 seconds, soak in 0.1% mercuric chloride for 6 minutes, then wash with sterile water for 4 times, and blot dry with sterile gauze for later use;
[0039] (2) Induction culture, cut off 2cm stem segments, cut off 2 / 3 of the needle length, and insert induction medium (induction medium is WPM basic medium + 6-BA0.5mg.L -1 +IBA0mg.L -1 + 30g.L sucrose -1 +Agar 7g.L -1 ), cultured in a dark incubator for 72 hours, and then placed in a light incubator, and the buds began to swell and ge...
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