Method for embryo culture in vitro and plant regeneration of euscaphis konishii hayata
The invention relates to a technology for cultivating the embryos of C. chinensis, which is applied in the directions of plant regeneration, botanical equipment and methods, horticultural methods, etc., and can solve the problems of short proliferation time, low seed germination rate, inability to provide tissue culture seedlings in large quantities, and the like, To achieve the effect of good growth and significant economic benefits
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[0021] Material collection method: select the seeds with full grains of the year, and wrap them with a damp cloth after picking;
[0022] Medium:
[0023] The MS basic medium was prepared using the formula in "Tissue Culture and Application of Woody Plants" published by Beijing Higher Education Press and edited by Chen Zhenghua in 1986.
[0024] The preparation of culture medium: basic medium is MS, add growth hormone to be BA, NAA, IAA, IBA, also add Su (sucrose) to be 20g / L in the medium, Ag + 7.5g / L, PH value is 5.8, the additive is activated carbon Ac; the thickness of the medium is generally 1.4 ~ 1.6cm;
[0025] Bud induction medium→MS+BA(1.0mg / L)+NAA(0.5 mg / L)+IAA(1.0mg / L)+Ag + (7.5g / L)+Su(20g / L)+Ac(2~2.5g / L)
[0026] Bud Proliferation Medium→MS+BA(2.0mg / L)+NAA(0.3mg / L)+IAA(1.0mg / L)+Ag + (7.5g / L)+Su(20g / L)+Ac(2~2.5g / L)
[0027] Rooting medium→1 / 2MS+NAA(0.1mg / L)+IBA(0.5mg / L)+Ag + (7.5g / L)+Su(20g / L)+Ac(2~2.5g / L)
[0028] Ag in medium + Derived from AgNO 3 .
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