Oil palm tissue culture breeding method
A tissue culture, oil palm technology, applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve the problems of shortening the tissue culture time of seedlings, unable to meet large-scale planting, low oil palm proliferation and differentiation rate, etc. The effect of shortening the cultivation time, short cultivation period and high rooting rate
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Embodiment 1
[0017] 1. Take 80 seed fruits collected 6 to 12 weeks after the flowering stage, which are basically the same size, have semi-red skin, and have not yet developed to the hard core stage. Wash them with tap water indoors, remove the pulp, cut the seed cores, and take out the ones with embryos. Endosperm pieces, first soaked in 70% alcohol for a few seconds, then rinsed with sterilized water 3 times, and then sterilized with saturated bleaching powder disinfectant for 10-30 minutes, the sterilized materials must be rinsed 3 times with sterile water Inoculated into callus induction medium (N 6 1 culture medium + activated carbon 3.0g / L + sucrose 30g / L + carrageenan 4.5g / L + 2,4-D 2.5mg / L), cultured in a dark room at 24°C for 80 days to obtain callus, The results are shown in Table 1. where N 6 1 Culture medium can refer to Ruslan Abdullah in the seventh issue of 2004 0717 ~ The Immature embryo: A useful tool for oil palm (Elaeis guineensis Jacq.) genetic transformation studies...
Embodiment 2
[0022] 1. Take 80 seed fruits collected 6 to 12 weeks after the flowering stage, which are basically the same size, have semi-red skin, and have not yet developed to the hard core stage. Wash them with tap water indoors, remove the pulp, cut the seed cores, and take out the ones with embryos. For the endosperm block, first soak it with 70% alcohol for 2-10 minutes, then rinse it with sterilized water for 3 times, and then soak it with 2% sodium hypochlorite solution for 10-20 minutes. Inoculate into callus induction medium (N 6 1 medium + activated carbon 3.0g / L + sucrose 30g / L + carrageenan 4.5g / L + 2,4-D 2.5mg / L), cultured in a dark room at 25°C for 75 days to obtain callus tissue, The results are shown in Table 1. where N 6 1 Culture medium can refer to Ruslan Abdullah in the seventh issue of 2004 0717 ~ The Immature embryo: A useful tool for oil palm (Elaeis guineensis Jacq.) genetic transformation studies published in Electronic Journal of Biotechnology in 3458 has the...
Embodiment 3
[0027] 1. Take 80 seed fruits collected 6 to 12 weeks after the flowering stage, which are basically the same size, have semi-red skin, and have not yet developed to the hard core stage. Wash them with tap water indoors, remove the pulp, cut the seed cores, and take out the ones with embryos. For the endosperm block, first soak it with 70% alcohol for a few seconds, then rinse it with sterilized water for 3 times, and then soak it with 2% sodium hypochlorite solution for 10-20 minutes. Inoculated into callus induction medium (N 6 1 medium + activated carbon 3.0g / L + sucrose 30g / L + carrageenan 4.5g / L + 2,4-D 2.5mg / L), cultured in a dark room at a temperature of 27°C for 65 days to obtain callus tissue, The results are shown in Table 1. where N 6 1 Culture medium can refer to Ruslan Abdullah in the seventh issue of 2004 0717 ~ The Immature embryo: A useful tool for oil palm (Elaeis guineensis Jacq.) genetic transformation studies published in Electronic Journal of Biotechnol...
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