Tissue culture method for Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher
A lampstand and white flower technology, which is applied in the field of plant tissue culture, can solve the problem of no white flower lamp, and achieve the effects of shortening the cultivation time, streamlining the process and saving costs
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Embodiment 1
[0023] The stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were used as explants for initial culture, multiplication and rooting culture, and the stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were selected and placed in tap water Add 2 drops of detergent to soak for 2 minutes, rinse with running tap water repeatedly for 10 minutes to remove surface impurities, then disinfect the surface with 75% alcohol, rinse with sterile water 5 times, and disinfect with 0.1% mercury liter solution for 7 minutes , rinsed repeatedly with sterile water for 3 times under sterile conditions, blotted the surface moisture with filter paper, cut off the damaged tissue, and inoculated the shoot tip into cluster bud induction medium MS+1.0mg / l ZT+1.0KT+0.2mg / l NAA, pH 5.8, start culture at 40% humidity and 20°C, inoculate 3 in each bottle; after 7 days, the callus grows and differentiates into cluster buds, and then transfers to the proliferation ...
Embodiment 2
[0027] The stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were used as explants for initial culture, multiplication and rooting culture, and the stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were selected and placed in tap water Add 3 drops of detergent to soak for 2 minutes, rinse with running tap water repeatedly for 10 minutes to remove surface impurities, then disinfect the surface with 75% alcohol, rinse with sterile water 4 times, and disinfect with 0.1% mercuric solution for 7 minutes , rinsed repeatedly with sterile water for 3 times under sterile conditions, blotted the surface moisture with filter paper, cut off the damaged tissue, and inoculated the shoot tip into cluster bud induction medium MS+1.0mg / l ZT+1.0KT+0.2mg / l NAA, pH 5.8, start the culture, inoculate 4 in each bottle; after 7 days, the callus grows and differentiates into cluster buds, and then transfers to the proliferation and rooting medium MS+1.5m...
Embodiment 3
[0031] The stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were used as explants for initial culture, multiplication and rooting culture, and the stem tips of Primula beesiana var. leucantha (Balf. f. et Forr.) Fletcher were selected and placed in tap water Add 3 drops of detergent to soak for 3 minutes, rinse with running tap water repeatedly for 10 minutes to remove surface impurities, then disinfect the surface with 75% alcohol, rinse with sterile water 5 times, and disinfect with 0.1% mercuric solution for 8 minutes , rinsed repeatedly with sterile water 5 times under sterile conditions, blotted the surface moisture with filter paper, cut off the damaged tissue, and inoculated the shoot tip into cluster bud induction medium MS+1.0mg / l ZT+1.0KT+0.2mg / l NAA, pH 5.8, for starting culture, inoculate 4 in each bottle; after 7 days, the callus grows and differentiates into cluster buds, and then transfers to the proliferation and rooting medium MS+1.5mg...
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