Ornithogalum arabicum Linn. tissue culture rapid breeding method
A white-flowered tiger eye and tissue culture technology, applied in the field of plant propagation, can solve the problems of difficult regeneration and low reproductive coefficient of bulbs, and achieve the effect of simple operation, high multiplication coefficient, and sustainable production and development
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Embodiment 1
[0045] Step 1, selection and processing of explants
[0046] Selecting the leaves of Dieffenbachia punctatus as a starting material, the collected leaves are cut into 3cm leaf segments as explants for tissue culture;
[0047] Step 2, the leaves are induced to form seedlings
[0048] Step 2-1, transfer the surface-sterilized leaf segments to a sterile inoculation tray, and dry the surface moisture of the leaf segments with sterile filter paper;
[0049] Step 2-2, place the sterilized leaf segment flat or insert it into the bulbil induction medium MS+TDZ2.0mg / L to induce bulbils, the culture temperature is 25°C, the light time is 14h / d, and the light intensity is 40u.Mol. m -2 .s -1 ; After a complete root system is gradually formed on the surface of the blade, the root system is inserted into the medium to become a new seedling;
[0050] The basic medium used is MS medium, the dosage of sucrose is 30g / L, the coagulant is agar powder, the dosage is 6.5g / L, and the pH of the ...
Embodiment 2
[0054] Step 1, selection and processing of explants
[0055] Selecting the leaves of Dieffenbachia vinifera as starting material, the collected leaves are cut into 2cm leaf segments as explants for tissue culture;
[0056] Step 2, the leaves are induced to form seedlings
[0057] Step 2-1, transfer the surface-sterilized leaf segments to a sterile inoculation tray, and dry the surface moisture of the leaf segments with sterile filter paper;
[0058] Step 2-2, place the sterilized leaf segment flat or insert it into the bulbil induction medium MS+TDZ2.0mg / L to induce bulbils, the culture temperature is 25°C, the light time is 13h / d, and the light intensity is 50u.Mol. m -2 .s -1 ; After a complete root system is gradually formed on the surface of the blade, the root system is inserted into the medium to become a new seedling;
[0059] The basic medium used is MS medium, the dosage of sucrose is 20g / L, the coagulant is agar powder, the dosage is 6g / L, and the pH of the mediu...
Embodiment 3
[0063] Step 1, selection and processing of explants
[0064] Selecting the leaves of Dieffenbachia vinifera as a starting material, the collected leaves are cut into 4cm leaf segments as explants for tissue culture;
[0065] Step 2, the leaves are induced to form seedlings
[0066] Step 2-1, transfer the surface-sterilized leaf segments to a sterile inoculation tray, and dry the surface moisture of the leaf segments with sterile filter paper;
[0067] Step 2-2, lay the sterilized leaf segments flat or insert them into the bulbil induction medium MS+TDZ2.0mg / L to induce bulbils, the culture temperature is 25°C, the light time is 12h / d, and the light intensity is 60u.Mol. m -2 .s -1 ; After a complete root system is gradually formed on the surface of the blade, the root system is inserted into the medium to become a new seedling;
[0068] The basic medium used is MS medium, the dosage of sucrose is 40g / L, the coagulant is agar powder, the dosage is 7g / L, and the pH of the me...
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