Haploid breeding method of dendrobium candidum
A technology of Dendrobium officinale and Dendrobium candidum, applied in the field of haploid breeding of Dendrobium officinale, can solve the problems of difficulty in guaranteeing the medicinal quality of Dendrobium officinale, hindering the sustainable development of Dendrobium candidum, resistance of varieties to diseases, poor resistance to retrograde, etc. and the development of high-quality varieties, huge potential commercial value, and the effect of improving the survival rate of embryos
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Embodiment 1
[0029] A haploid breeding method of dendrobium officinale, comprising the steps of:
[0030] a. Get the flowers of Dendrobium officinale that have bloomed for 3-6 days, inoculate pollen at normal temperature before cultivating, and treat them in an anther callus induction medium at a low temperature of 4°C for 48 hours, and then carry out conventional culture;
[0031] b. Sterilize with a 5.6% NaCIO solution for 15 minutes, rinse with sterile water for 5 times, peel off the anthers from the sterilized flower buds in a sterile environment, try to prevent the anthers from being damaged, and inoculate them in the anther callus induction culture Base, seal with plastic wrap;
[0032] c. Carry out dark constant temperature culture at 25°C for 2-3 days, and then carry out dark shaking culture for 12-15 days to obtain embryoid bodies;
[0033] d. Collect the embryoid body, inoculate it into the differentiation medium, and then cultivate it in the tissue culture room under light for ...
Embodiment 2
[0039] A haploid breeding method of dendrobium officinale, comprising the steps of:
[0040] a. Get the flowers of Dendrobium officinale that have bloomed for 3-6 days, inoculate pollen at normal temperature before cultivating, and treat them in an anther callus induction medium at a low temperature of 4°C for 48 hours, and then carry out conventional culture;
[0041] b. Sterilize with a 5.6% NaCIO solution for 15 minutes, rinse with sterile water for 5 times, peel off the anthers from the sterilized flower buds in a sterile environment, try to prevent the anthers from being damaged, and inoculate them in the anther callus induction culture Base, seal with plastic wrap;
[0042] c. Carry out dark constant temperature culture at 25°C for 2-3 days, and then carry out dark shaking culture for 12-15 days to obtain embryoid bodies;
[0043]d. Collect the embryoid body, inoculate it into the differentiation medium, and then cultivate it in the tissue culture room under light for 1...
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