Tissue culture method of acer rubrum
A safflower maple, tissue culture technology, applied in horticultural methods, botanical equipment and methods, horticulture, etc., to achieve the effects of low pollution rate, scientific steps, and high induction rate
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Embodiment 1
[0031] This embodiment discloses a method for tissue culture of Acer safflower, comprising the following steps:
[0032] Step 1, cut the dormant buds of the Acer japonica plant individual and carry out pretreatment, then inoculate on the induction medium containing 0.05mg / L cytokinin, 0.05mg / L auxin, 30g / L sucrose and 6g / L agar, At a temperature of 25°C, a humidity of 60%, and a light intensity of 50 μmol m -2 ·s -1 , 20 hours of light per day, 20 days to obtain sterile sprouts;
[0033] Step 2: Cut the obtained sterile sprouts into 1.5-3.0cm stem segments with terminal buds, inoculate them with 0.05mg / L cytokinin, 0.05mg / L auxin, 30g / L sucrose and 6g / L On the induction medium of agar, at a temperature of 25°C, a humidity of 60%, and a light intensity of 800 μmol·m -2 ·s -1 1. Cultivate for 2 months under the conditions of 18 hours of light per day and replacement of fresh medium every 25 days to obtain clustered sprouts;
[0034] Step 3: Select the strong clustered sprouts...
Embodiment 2
[0040] This embodiment discloses a method for tissue culture of Acer safflower, comprising the following steps:
[0041] Step 1, cut the dormant buds of the Acer japonica plant individual and carry out pretreatment, then inoculate on the induction medium containing 0.1mg / L cytokinin, 0.08mg / L auxin, 20g / L sucrose and 7g / L agar, At a temperature of 20°C, a humidity of 60%, and a light intensity of 20 μmol m -2 ·s -1 , 12 hours of light per day, 30 days to obtain sterile sprouts;
[0042] Step 2: Cut the obtained sterile sprouts into 1.5-3.0cm stem segments with terminal buds, inoculate them with 0.03mg / L cytokinin, 0.05mg / L auxin, 20g / L sucrose and 7g / L On the induction medium of agar, at a temperature of 30°C, a humidity of 80%, and a light intensity of 20 μmol·m -2 ·s -1 1. Cultivate for 1 to 3 months under the conditions of 12 hours of light per day and replacement of fresh medium every 30 days to obtain clustered sprouts;
[0043] Step 3: Select the strong clustered sp...
Embodiment 3
[0049] This embodiment discloses a method for tissue culture of Acer safflower, comprising the following steps:
[0050] Step 1, cut the dormant buds of the Acer japonica plant individual and carry out pretreatment, then inoculate on the induction medium containing 0.02mg / L cytokinin, 0.05mg / L auxin, 20g / L sucrose and 5g / L agar, At a temperature of 20°C, a humidity of 70%, and a light intensity of 20 μmol m -2 ·s -1 , 24h and 30 days of light every day to obtain sterile sprouts;
[0051] Step 2: Cut the obtained sterile sprouts into 1.5-3.0cm stem segments with terminal buds, inoculate them with 0.06mg / L cytokinin, 0.08mg / L auxin, 35g / L sucrose and 5g / L On the induction medium of agar, at a temperature of 25°C, a humidity of 50%, and a light intensity of 80 μmol·m -2 ·s -1 1. Cultivate for 2 months under the conditions of 15 hours of light per day and replacement of fresh medium every 30 days to obtain clustered sprouts;
[0052] Step 3: Select the strong clustered sprout...
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