Rapid propagation method for flos farfarae
A fast technology for coltsfoot flower, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of low reproduction efficiency of coltsfoot flower rhizome and limit the rapid development of coltsfoot flower industry, and achieve good application prospects and cycle time Short, fast growing effect
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Embodiment 1
[0017] In the late autumn and early winter seasons, choose coltsfoot rhizomes that are thick and multi-flowered, white in color, and free from diseases and insect pests, wash the attached soil with clean water, add a few drops of Tween 80 to 0.1% mercury solution and soak for 10 minutes, and then use Rinse with sterile water three times, each time for 2min, cut into small sections of 1cm as explants, inoculate the explants in the induction medium and carry out cluster bud induction culture under light conditions to obtain cluster buds; the induction medium is MS The medium was used as the basic medium, and the macroelements were halved, and sucrose at a concentration of 15g / L, agar at a concentration of 2g / L, 6-BA at a concentration of 0.5mg / L, and NAA at a concentration of 0.3mg / L were added. The clustered buds are transferred to the proliferation medium to carry out the subculture of the clustered buds under light conditions to obtain the subcultured proliferation of the clus...
Embodiment 2
[0019] In the late autumn and early winter seasons, choose coltsfoot rhizomes that are thick and multi-flowered, white in color, and free from diseases and insect pests, wash the attached soil with clean water, add a few drops of Tween 80 to 0.1% mercury solution and soak for 10 minutes, and then use Rinse with sterile water three times, each time for 5min, cut into small sections of 2cm as explants, inoculate the explants in the induction medium and carry out cluster bud induction culture under light conditions to obtain cluster buds; the induction medium is MS The medium was used as the basic medium, and the macroelements were halved, and 25 g / L sucrose, 5 g / L agar, 1.5 mg / L 6-BA, and 1 mg / L NAA were added. The clustered buds are transferred to the proliferation medium and carried out the subculture of the clustered buds under light conditions to obtain the subsequent proliferation of the clustered buds; the proliferation medium uses MS (1 / 3NH4N03) medium as the basic medium,...
Embodiment 3
[0021] In the late autumn and early winter seasons, choose coltsfoot rhizomes that are thick and multi-flowered, white in color, and free from diseases and insect pests, wash the attached soil with clean water, add a few drops of Tween 80 to 0.1% mercury solution and soak for 10 minutes, and then use Rinse with sterile water three times, each time for 3 minutes, cut into small sections of 1-2 cm as explants, inoculate the explants in the induction medium and carry out cluster bud induction culture under light conditions to obtain cluster buds; the induction medium MS medium was used as the basic medium, macronutrients were halved, and sucrose at a concentration of 20g / L, agar at a concentration of 3.5g / L, 6-BA at a concentration of 1.2mg / L, and 0.6mg / L were added The NAA. The clustered buds are transferred to the proliferation medium to carry out the subculture of the clustered buds under light conditions to obtain the subcultured proliferation of the clustered buds; the proli...
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