A cultivation method for rapidly obtaining regenerated seedlings of Lycium barbarum
A technology of black fruit wolfberry and cultivation method, which is applied in the field of tree biology, can solve the problems of low bud formation rate and long cultivation time, and achieve the effects of reducing cultivation cost, fast growth speed and strong root system
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experiment example 1
[0047] Experimental example 1: MS medium configuration
[0048] S1: MS medium stock solution configuration
[0049] Contrast Table 1-4, weigh each component respectively.
[0050] Table 1: MS macroelement mother liquor formula
[0051]
[0052] After weighing, dissolve thoroughly with a small amount of distilled water and mix, and finally make up to 1L.
[0053] Table 2: MS trace element mother liquor formula
[0054]
[0055] After weighing, dissolve thoroughly with a small amount of distilled water and mix, and finally make up to 1L.
[0056] Table 3: MS inositol master solution formula
[0057]
[0058] After weighing, dissolve thoroughly with a small amount of distilled water and mix, and finally make up to 1L.
[0059] Table 4: Formula of MS iron salt mother liquor
[0060]
[0061] After weighing, dissolve thoroughly with a small amount of distilled water and mix, and finally make up to 1L.
[0062] S2: MS medium configuration
[0063] Dilute the MS t...
experiment example 2
[0064] Experimental example 2: The configuration of hormone NAA and 6-BA
[0065] Weigh 0.04g of NAA powder, dissolve it with 1ml of absolute ethanol, and then set the volume to 200ml to obtain a 0.2mg / ml NAA solution, and store it in a refrigerator at 4°C for later use.
[0066] Weigh 0.04g of 6-BA powder, dissolve it with 1mol / L dilute sodium hydroxide solution, and then set the volume to 200ml to obtain a 0.2mg / ml 6-BA solution, and then store it in a refrigerator at 4°C for later use.
Embodiment 1
[0068] 1. Disinfection of seeds
[0069] Select black wolfberry seeds, soak them in 70v% alcohol for 5 minutes, then disinfect them with 0.1wt% mercuric chloride solution for 15 minutes, and then rinse them three times with sterile water.
[0070] 2. Obtaining sterile seedlings
[0071] Add 30g sucrose and 8.0g agar to each liter of MS medium, adjust the pH value to 5.8 with 1mol / L NaOH solution, and then sterilize under high pressure at 121°C for 15min to obtain MS-0 medium, at this time the pH of the medium The value is 5.2.
[0072] The seeds in step 1 are placed in MS-0 medium, and sterile seedlings are obtained after the seeds germinate for 8-12 days.
[0073] 3. Induction of Callus
[0074] Add 1.0 mg NAA, 2.0 mg 6-BA, 30 g sucrose and 8.0 g agar to each liter of MS medium, adjust the pH value to 5.8 with 1 mol / L NaOH solution, and then sterilize under high pressure at 121°C for 15 minutes to obtain MS-0 Culture medium, the pH value of the culture medium at this time...
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