Hydrangea macrophylla-polar bear (a variety of hydrangea macrophylla) tissue culture medium and culture method
A tissue culture and culture method technology, applied in the medium and culture field of hydrangea-polar bear tissue culture, can solve the problems of low high-quality commodity rate and inability to reproduce quickly, achieve high commodity rate, improve reproduction speed and seedling uniformity , the effect of reducing production costs
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Embodiment 1
[0022] A cultivation method for hydrangea-polar bear tissue culture, comprising the following steps:
[0023] (1) Obtaining sterile materials: select explants with good growth and no tender branches of diseases and insect pests, remove the leaves of the explants, lightly brush to remove the surface fluff, soak in clean water with detergent for no more than 1 minute, and then rinse The explants were filtered until there was no foam; on the ultra-clean workbench, sterilized with a prepared mixed solution of 0.08% mercuric chloride and Tween for 10 minutes, rinsed with sterile water 4 times, filtered to dry, and sterilized The finished explants are cut off the wound and the injured part, cut into length 2cm stem segments with axillary buds, inserted into the prepared medium and cultivated for 9 days;
[0024] (2) Bud induction: the axillary bud induction medium is 1 / 2WPM+6-BA 1mg / L+2,4-D 0.1 mg / L, pH 5.8, temperature 24°C, light intensity 2300lx, light Alternate with dark cultur...
Embodiment 2
[0029] A cultivation method for hydrangea-polar bear tissue culture, comprising the following steps:
[0030] (1) Obtaining sterile materials: select explants with good growth and no tender branches of diseases and insect pests, remove the leaves of the explants, lightly brush to remove the surface fluff, soak in clean water with detergent for no more than 1 minute, and then rinse The explants were filtered until there was no foam; on the ultra-clean workbench, sterilized with a prepared mixed solution of 0.09% mercuric chloride and Tween for 6 minutes, rinsed with sterile water for 4 times, dried the water, and sterilized The finished explant is cut off the wound and the injured part, cut into a stem section with axillary buds of 2 cm in length, inserted into the prepared medium and cultivated for 8 days;
[0031] (2) Bud induction: the axillary bud induction medium is 1 / 2WPM+6-BA1.25 mg / L+2,4-D 0.1 mg / L, pH is 5.8, temperature is 25°C, light intensity is 2500lx , light and ...
Embodiment 3
[0036] A cultivation method for hydrangea-polar bear tissue culture, comprising the following steps:
[0037] (1) Obtaining sterile materials: select explants with good growth and no tender branches of diseases and insect pests, remove the leaves of the explants, lightly brush to remove the surface fluff, soak in clean water with detergent for no more than 1 minute, and then rinse The explants were filtered until there was no foam; on the ultra-clean workbench, sterilized with a prepared mixed solution of 0.1% mercuric chloride and Tween for 8 minutes, rinsed with sterile water for 6 times, drained the water, and sterilized The finished explant is cut off the wound and the injured part, cut into a stem segment with axillary buds of 2 cm in length, inserted into the prepared medium and cultivated for 7 days;
[0038] (2) Bud induction: the axillary bud induction medium is 1 / 2WPM+6-BA 1.5 mg / L+2,4-D 0.1 mg / L, pH is 5.8, temperature is 23°C, light intensity is 2700lx, Alternate ...
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