Tissue culture method of dianthus deltoids
A technology of girl dianthus, cultivation method, applied in gardening methods, botanical equipment and methods, horticulture and other directions, can solve the problems of degradation, quality of disease infection, less seedlings in seedling cultivation time, etc.
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Embodiment 1
[0033] Embodiment 1. The influence of the selection and operation method of the girl carnation explant on the induction of adventitious buds
[0034] The dianthus used in the experiment was collected from the experimental nursery of the Drought Resistant Plant Research Institute of Hexinyuan Mengcao Drought Resistant Greening Co., Ltd. in Inner Mongolia. According to the progress of the experiment, samples were taken at different times and supplemented at any time. Harvest the stem tips of young dianthus shoots about 0.5-1.0cm long, wash them with running water, soak them in 70% alcohol for 10 seconds, then disinfect them with 0.1% mercury liter for 5 minutes, rinse them twice with sterile water, 5 minutes each time , inoculated on the improved primary medium (MS) to establish a clone of test-tube plantlets. Select the clustered buds of about 10 days of subculture, cut off the base of the clustered buds; take the shoot tips of the clustered buds, about 0.5-1.0 cm in length, as...
Embodiment 2
[0041] Example 2. Screening of optimal medium for each stage of girl carnation tissue culture
[0042] 1. Statistical calculation formula of screening effect
[0043] Survival rate = (number of viable explants / total number of inoculated explants) × 100%
[0044] Primary bud induction rate=(number of explants that germinated / total number of inoculated explants)×100%
[0045] Multiplication multiple of subculture = (number of clustered buds induced / total number of buds inserted into a single plant) × 100%
[0046] Rooting rate = (number of explants with differentiated roots / total number of inoculated explants) × 100%
[0047] 2. Selection of the best medium for each stage of Dianthus tissue culture
[0048] MS was used as the basic medium, 3.5g / L carrageenan was used as the solidifying agent, 3% edible sugar was used as the carbon source instead of sucrose, tap water was used instead of distilled water, and different ratios of cytokinin and auxin were added to the culture m...
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