Method for in vitro culture of hemerocallis middendorfii Trautv. et Mey. tissue
A technology for in vitro cultivation of Hemerocallis grandiflorum, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of large market demand, small number of introduced species, slow division, etc. The uniformity, cost reduction, and the effect of maintaining the traits of the female parent
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Embodiment 1
[0025] A method for in vitro tissue culture of Hemerocallis grandiflora, comprising the following steps:
[0026] (1) The preparation of the culture medium in each culture stage, including the components and contents of the culture medium:
[0027] Bud induction medium: MS+KT0.3mg / L+6-BA2.0mg / L+NAA1mg / L;
[0028] Adventitious bud proliferation medium: MS+6-BA2.0mg / L+NAA0.1mg / L;
[0029] Strong seedling medium: MS+6-BA0.5mg / L+NAA0.05mg / L;
[0030] Rooting medium: MS+NAA0.05mg / ;
[0031] Each of the above media also includes the following components: 30 g / L sucrose, 6 g / L agar; the pH value in the media is 5.8.
[0032] (1) Obtaining sterile materials: Pick the small buds on the flower stems of Hemerocallis grandiflora during the flowering season, wash them with tap water for 1 hour, place them on a clean bench, soak them in 75wt% ethanol for 30s, and use 1wt‰ Soak in mercuric chloride for 15 minutes, rinse with sterile water for 5-6 times, blot the surface with sterile filt...
Embodiment 2
[0039] A method for in vitro tissue culture of Hemerocallis grandiflora, comprising the following steps:
[0040] (1) The preparation of the culture medium in each culture stage, including the components and contents of the culture medium:
[0041] Bud induction medium: MS+KT0.5mg / L+6-BA3.0mg / L+NAA2mg / L;
[0042] Adventitious bud proliferation medium: MS+6-BA3.0mg / L+NAA0.3mg / L;
[0043] Strong seedling medium: MS+6-BA2.0mg / L+NAA0.2mg / L;
[0044] Rooting medium: MS+NAA0.2mg / ;
[0045] Each of the above media also includes the following components: 30 g / L sucrose, 6 g / L agar; the pH value in the media is 5.8.
[0046] (1) Obtaining sterile materials: Pick the small buds on the flower stems of Hemerocallis grandiflora during the flowering season, wash them with tap water for 1 hour, place them on a clean bench, soak them in 75wt% ethanol for 30s, and use 1wt‰ Soak in mercuric chloride for 15 minutes, rinse with sterile water for 5-6 times, blot the surface with sterile filter...
Embodiment 3
[0053] A method for in vitro tissue culture of Hemerocallis grandiflora, comprising the following steps:
[0054] (1) The preparation of the culture medium in each culture stage, including the components and contents of the culture medium:
[0055] Bud induction medium: MS+KT0.4mg / L+6-BA2.5mg / L+NAA1.5mg / L;
[0056] Adventitious bud proliferation medium: MS+6-BA2.5mg / L+NAA0.2mg / L;
[0057] Strong seedling medium: MS+6-BA1mg / L+NAA0.1mg / L;
[0058] Rooting medium: MS+NAA0.1mg / ;
[0059] Each of the above media also includes the following components: 30 g / L sucrose, 6 g / L agar; the pH value in the media is 5.8.
[0060] (1) Obtaining sterile materials: Pick the small buds on the flower stems of Hemerocallis grandiflora during the flowering season, wash them with tap water for 1 hour, place them on a clean bench, soak them in 75wt% ethanol for 30s, and use 1wt‰ Soak in mercuric chloride for 15 minutes, rinse with sterile water for 5-6 times, blot the surface with sterile filter...
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