A method of callus induction and tissue culture seedling rapid propagation
A technique for inducing callus and fetus is applied in the field of plant biology, and can solve the problems of hindering the application of fetus tissue culture seedlings, low proliferation coefficient and high culture cost, and achieves protection of ecological environment diversity, simple operation and low production cost. Effect
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Embodiment 1
[0026] A method for induction of Zouma fetus callus and rapid propagation of tissue culture seedlings, comprising the following steps:
[0027] (1) On the ultra-clean workbench, sterilize the seeds of Zoumatai with 75% ethanol solution for 1 min, wash with sterile water once, and then use 0.1% mercury chloride (HgCl 2 ) solution was sterilized for 10 min, washed with sterile water for 5 times, placed on sterilized filter paper to absorb water, inserted into MS medium and cultured for 40 days, and the seeds germinated to obtain sterile plants; the stems of sterile plants The segments and shoots were cultured on the callus induction medium for 40 days, and the induction rate was 100%;
[0028] The callus induction medium is: MS+2,4-D0.5 mg / L+6-BA0.1 mg / L+sucrose 20 g / L+agar 5 g / L, pH value is 5.8;
[0029] (2) On the ultra-clean workbench, cut the callus induced by the stem segment and bud of Zouma fetus into 0.2 cm × 0.2 cm small pieces, insert it into the proliferation medium...
Embodiment 2
[0039] A method for induction of Zouma fetus callus and rapid propagation of tissue culture seedlings, comprising the following steps:
[0040] (1) On the ultra-clean workbench, sterilize the seeds of Zoumatai with 75% ethanol solution for 1 min, wash with sterile water once, and then use 0.1% mercury chloride (HgCl 2 ) solution was sterilized for 10 min, washed with sterile water for 5 times, placed on sterilized filter paper to absorb water, inserted into MS medium and cultured for 40 days, and the seeds germinated to obtain sterile plants; the stems of sterile plants The segments and shoots were cultured on the callus induction medium for 40 days, and the induction rate was 100%;
[0041]The callus induction medium is: MS+2,4-D0.5 mg / L+6-BA0.1 mg / L+sucrose 20 g / L+agar 5 g / L, pH value is 5.8;
[0042] (2) On the ultra-clean workbench, cut the callus induced by the stem segment and bud of Zouma fetus into 0.2 cm × 0.2 cm small pieces, insert it into the proliferation medium ...
Embodiment 3
[0052] A method for induction of Zouma fetus callus and rapid propagation of tissue culture seedlings, comprising the following steps:
[0053] (1) On the ultra-clean workbench, sterilize the seeds of Zoumatai with 75% ethanol solution for 1 min, wash with sterile water once, and then use 0.1% mercury chloride (HgCl 2 ) solution was sterilized for 10 min, washed with sterile water for 5 times, placed on sterilized filter paper to absorb water, inserted into MS medium and cultured for 40 days, and the seeds germinated to obtain sterile plants; the stems of sterile plants The segments and shoots were cultured on the callus induction medium for 40 days, and the induction rate was 100%;
[0054] The callus induction medium is: MS+2,4-D0.5 mg / L+6-BA0.1 mg / L+sucrose 20 g / L+agar 5 g / L, pH value is 5.8;
[0055] (2) On the ultra-clean workbench, cut the callus induced by the stem segment and bud of Zouma fetus into 0.2 cm × 0.2 cm small pieces, insert them into the proliferation medi...
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