Rapid propagation method for tissue cultivation of dendrobium candidum stem
A technology for Dendrobium officinale and stem segments, which is applied to the field of rapid tissue culture propagation of Dendrobium officinale stem segments, can solve the problems of long reproductive cycle, low multiplying multiples, limited maternal traits, etc., and achieves good economic and social benefits and stable genetic traits. , the effect of maintaining the characteristics of the mother
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Embodiment 1
[0019] Select a single plant stem with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, wash the whole section of fresh strips and air-dry to remove 40% of the water in the fresh strips; Under the condition of bacteria, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, then rinse them with sterile water for 6 times, and then absorb the explants with sterile filter paper After burning the water on the surface of the implant, cut it into a stem segment with one node; cut off both ends of the stem segment, and inoculate it into the following induction medium: 1 / 2MS+0.5mg / L6- BA+0.2mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.4; the culture temperature for induction culture is 22℃, and the light intensity is 1600Lux, the light time is 8 hours / day, and t...
Embodiment 2
[0021] Select a single plant stem with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, and the whole section of fresh strips is washed and air-dried to remove 35% of the water in the fresh strips; Under the condition of bacteria, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, then rinse them with sterile water for 6 times, and then absorb the explants with sterile filter paper After burning on the flame of an alcohol lamp, cut into a stem segment with one node; cut off both ends of the stem segment, and inoculate into the following induction medium: 1 / 2MS+1.0mg / L6-BA +0.5mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.6; the culture temperature for induction culture is 28℃, and the light intensity is 2000Lux , the light time is 8 hours / day, and the...
Embodiment 3
[0023]Select the stems of a single plant with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, and the whole section of fresh strips is washed and air-dried to remove 45% of the water in the fresh strips; Under the condition of bacteria, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, then rinse them with sterile water for 6 times, and then absorb the explants with sterile filter paper After burning on the flame of an alcohol lamp, cut into a stem segment with one node; cut off both ends of the stem segment, and inoculate into the following induction medium: 1 / 2MS+0.8mg / L6-BA +0.2mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.2; the culture temperature during induction culture is 25℃, and the light intensity is 1800Lux , the light time is 8 hours / da...
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