Rapid breeding method of senecio cruentus
A cineraria, rapid technology, applied in the field of plant tissue culture, can solve the problems of unfavorable in vitro tissue regeneration large-scale culture, poor stability of regeneration system, low germination rate of somatic embryos, etc., and achieves the promotion of callus growth and regeneration. The effect of stable system and high transplanting survival rate
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Embodiment 1
[0050] 1. Test materials
[0051] 1. Mature cineraria 'Joker' seeds come from Gold Smith Company in the United States.
[0052] The five varieties of cineraria 'clown' used in the embodiments of the present invention are respectively: blue, white, pink, scarlet and yellow.
[0053] 2. Plant growth regulator
[0054] The plant growth regulating substance used in the present invention adopts domestic indole butyric acid (IBA), naphthaleneacetic acid (NAA), 6-benzylaminoadenine (6-BA) and 2,4-dichlorophenoxyacetic acid (2 , 4-D).
[0055] 3. Preparation of culture medium:
[0056] (1) The composition or preparation method of "MS basic medium";
[0057] Table 1 MS medium (Murashige and Skoog, 1962)
[0058] MS macroelements
Mother liquor composition
content
(g / L)
MS trace elements
Mother liquor composition
content
(g / L)
Mother liquor composition
content
(g / L)
NH4NO3
33
h 3 BO ...
Embodiment 2
[0093] The seeds of scarlet cineraria 'clown' were used for sterile seedling cultivation; the 6-BA used in the cluster bud induction medium was 0.5 mg / L, and the NAA was 0 mg / L; the 6-BA used in the callus induction medium was 2.0mg / L, NAA 3.0mg / L, 2,4-D 0.5mg / L; 6-BA used in callus proliferation medium 0.5mg / L, NAA 0.5mg / L; Adventitious bud differentiation The 6-BA used in the medium is 2.0mg / L, the NAA is 3.0mg / L, and the 2,4-D is 0.5mg / L; the IBA used in the rooting medium of adventitious roots is 0.1mg / L, and the others are the same as those of the implementation Example 1 is the same.
Embodiment 3
[0095] Seeds of blue cineraria 'clown' were used for sterile seedling culture; 6-BA used in the cluster bud induction medium was 1.0 mg / L, and NAA was 0.1 mg / L; 6-BA used in the callus induction medium 3.0mg / L, NAA 2.0mg / L, 2,4-D 0.5mg / L; 6-BA used in callus proliferation medium was 1.0mg / L, NAA 0.5mg / L; adventitious buds The 6-BA used in the differentiation medium is 3.0mg / L, the NAA is 2.0mg / L, and the 2,4-D is 0.5mg / L; the NAA used in the rooting medium of adventitious roots is 0.1mg / L, and the others are the same as Example 1 is the same.
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