A kind of culture medium group and its application of the tissue culture rapid propagation of the plant
A technology of tissue culture rapid propagation and medium, applied in the application, plant regeneration, plant cells and other directions, can solve the problems of browning of tissue materials, high seed reproduction efficiency, difficult to collect, etc., to promote shoot rooting, efficient induction of healing. The effect of wounding tissue and efficiently inducing the formation and growth of buds
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Embodiment 1
[0041] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.
[0042] Among them, the induction medium includes 0.8MS medium, 6-BA 0.5mg / L, IAA 0.1mg / L, 2,4-D0.1mg / L, sucrose 30g / L, agar 5g / L, Vc 0.2mg / L , Sodium nitrosoferricyanide 2.0mg / L, pH=5.6;
[0043] Differentiation medium includes 1.5MS medium, 6-BA 0.8mg / L, NAA 0.1mg / L, IAA 0.1mg / L, sucrose 30g / L, agar 5g / L, pH=6.2;
[0044] Rooting medium includes 0.8MS medium, NAA 0.15mg / L, IBA 0.025mg / L, sucrose 20g / L, agar 5g / L, potato juice 2.0mL / L, activated carbon 1g / L, pH=5.8.
[0045] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid
[0046] Among them, the induction medium is used to induce culture of the explants of Maojiancao to obtain callus (the callus rate is 86.85%); the differentiation medium is used to differentiate and cultivate the callus to...
Embodiment 2
[0048] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.
[0049] Among them, the induction medium includes 1.5MS medium, 6-BA 1.0mg / L, IAA 0.3mg / L, 2,4-D 0.2mg / L, sucrose 30g / L, agar 5g / L, Vc 0.4mg / L , Sodium nitroferricyanide 6.0mg / L, pH=6.2;
[0050] Differentiation medium includes 0.8MS medium, 6-BA 0.5mg / L, NAA 0.05mg / L, IAA 0.05mg / L, sucrose 30g / L, agar 5g / L, pH=5.6;
[0051] Rooting medium includes 1.0MS medium, NAA 0.2mg / L, IBA 0.05mg / L, sucrose 25g / L, agar 5g / L, potato juice 3.0mL / L, activated carbon 1g / L, pH=6.2.
[0052] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid
[0053] Among them, the induction medium is used to induce the explants of Maojiancao to obtain callus (the callus rate is 94.48%); the differentiation medium is used to differentiate and cultivate the callus to obtain adve...
Embodiment 3
[0055] 1. a culture medium group of the tissue culture rapid propagation of blue orchid plant, comprise induction medium, differentiation medium and rooting medium.
[0056] Among them, the induction medium includes MS medium, 6-BA 0.8mg / L, IAA 0.2mg / L, 2,4-D 0.15mg / L, sucrose 30g / L, agar 5g / L, Vc 0.3mg / L, Sodium nitrosoferricyanide 4.0mg / L, pH=5.8;
[0057] Differentiation medium includes MS medium, 6-BA 0.7mg / L, NAA 0.08mg / L, IAA 0.08mg / L, sucrose 30g / L, agar 5g / L, pH=5.8;
[0058] Rooting medium includes 0.5MS medium, NAA 0.1mg / L, sucrose 15g / L, agar 5g / L, potato juice 1.0mL / L, activated carbon 1g / L, pH=5.6.
[0059] 2. The application method of the culture medium group of the tissue culture rapid propagation of a kind of blue orchid
[0060] Wherein, the induction medium is used for inducing culture to the explant of Mao Jiancao, to obtain callus (the callus rate is 88.15%); Differentiation medium is used for the differentiation culture of callus, to obtain adventitious ...
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