• 正交设计可提高试验效率准确性愈伤组织诱导培养基分化培养基筛选优化方法

    Orthogonal design improved experimental efficiency and precision, which was a good way for selection and optimization of callus induction medium and differentiation medium.

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  • 对于伤组织再分化不仅需要细胞分裂素而且诱导培养基生长素浓度影响也是显著的。

    With regard to the callus redifferentiation, not only kinetin is needed, but also the effect of auxin concentration of the induction medium is also remarkable.

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  • MS培养基加入不同植物激素研究果腺肋花楸叶片愈伤组织诱导及其再分化。

    Callus induction and redifferentiation of black chokeberry leaf in vitro were studied when a diversity of plant hormones were added to MS media.

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  • 采用正交设计方法,研究了NAA6-BAMS培养基对明党参叶片叶柄愈伤组织诱导影响。

    Effects of NAA, 6-BA, MS culture medium on leaf and petiole callus induction of Changium smyrnioides Wolff were studied by orthogonal design.

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  • 原生质体培养基诱导伤组织

    They were induced to small calli in the medium.

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  • 利用水稻成熟外植体,接种NB培养基上,分别附加不同外源激素,以诱导愈伤组织并促其分化,最终获得水稻再生植株。

    The mature embryos were cultivated on NB media with different hormones, by using the mature embryos in rice as explants, and regeneration plants were obtained successfully.

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  • 选择合适的水稻起始材料选用适宜培养基配方对于水稻花培愈伤组织诱导分化至关重要。

    It was important for callus induction and shoot differentiation to choose better starting materials and a suitable medium in rice anther culture.

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  • 转化细胞来自白花曼陀罗LS固体培养基诱导产生愈伤组织

    Cultured cells derived from stems of Datura stramonium were maintained in Linsmaiher and Skoog (ls) solid medium.

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  • 大叶黄杨外植体添加BANAAIBA2,4-D不同激素组合MS培养基上培养,对其伤组织进行诱导试验。

    With young stem segment of Euonymus japonicus as explants, callus induction were studied on MS basal medium supplemented with different hormone combinations including BA and NAA, IBA , 2,4-D.

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  • M6培养基适于侧芽生长皮下组织诱导愈伤

    M6 medium was suitable for growth of side-bud and callus Induction of subcutaneous tissue.

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  • 方法:将丹参外植体培养不同激素配比诱导培养基,并对伤组织所含次生代谢产物进行分析。

    Method:Study the development of allochtonic formations in the callus from explants of Salvia miltiorrhiza cultured on hormones of different content ratios in the medium.

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  • 玉米自交系4112胚为外植体,MS基本培养基研究了不同质量浓度2,4 - D愈伤组织诱导影响

    Influence of different mass concentration of 2, 4-d on callus induction in maize inbred line 4112 from immature embryos with MS being used as basal culture medium was studied.

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  • 以美国黑树莓叶片作为外植体,以MS为基本培养基,添加不同浓度6-BA、NAAIAA进行愈伤组织诱导植株再生试验。

    The leaves of the blackberry as the explant, and MS contained different concentration of 6-BA, NAA or IAA as the media, the callus induction and the plant regeneration of the blackberry were studied.

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  • 培养基类型伤组织诱导分化明显影响MS培养基优于DCR培养基

    Media had obvious effect on calli induction and differentiation. MS medium was better than DCR medium.

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  • 结果表明,以体去皮为外植体,MS为基本培养基诱导愈伤组织较为适宜。

    Callus was efficiently induced from in vitro root segment devoid of rhizodermis on MS medium.

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  • 以金边瑞香段为外植体,探讨了不同培养基伤组织诱导愈伤组织分化的影响。

    These young stems as explants placed on different media formed calli, whose amount then increased by different cultures on different media and for different generations.

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  • 在不添加2,4 - D培养基外植体愈伤组织诱导并且需要诱导长的时间

    Without added 2, 4-d in the medium, explant callus induction rate is very low, and needed a very long time to induct.

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  • 培养基上均不能诱导伤组织

    The callus from stem segments can not induced in the medium added to NaCl.

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  • W14 是适合花药愈伤组织诱导基本培养基

    W14 was the best basal media for the first step of callus induction.

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  • 继代培养30 d铁皮石斛类原球茎作接种材料,以N6基本培养基加入植物激素以真菌提取物诱导子,类原球茎愈伤组织进行诱导培养。

    Methods Protocorm-like bodies and callus of DCWL subcultured for 30 days was used as the explants, N6 was used as the basic culture with phytohormone added, and fungal extracts as the elicitor.

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  • 伤组织转移到体细胞诱导培养基诱导出体细胞

    Somatic embryos could be induced after the embryogenic calli were transplanted on somatic embryo induction medium.

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  • 红枫腋芽培养基诱导愈伤组织增殖分化

    The bud can easily produce calli and propagate but has no differentiation on the culture medium.

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  • 结果表明CC培养基绝大多数水稻伤组织诱导继代培养基

    The main results were as following: For most rice CC medium was the best for both callus initiation and subculture.

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  • 伤组织诱导过程比较了不同基本培养基、不同浓度的激素组合、不同外植体的影响。

    In the course of calli induction, different basal media, combination of plant growth regulators and explants were compared.

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  • 试验还得到唐菖蒲“超级玫瑰球茎诱导伤组织最佳培养基愈伤组织生长最适培养基

    The effects of electron beam and fast neutrons on the callus induction of corm of gladiolus"Rose Supreme"were investigated by using the orthogonal experiment design.

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  • 结果:将愈伤组织接种含有0。2%秋水仙培养基上,通过培养形成的多倍体植株诱导为12。

    Result: The polyploid of P. chinense was obtained using calli with stem treated with 0.2% colchicines medium, the inducing rate reached 12.45%.

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  • 实验结果表明MS为基本培养基,在诱导培养基中加入2,4-D利于愈伤组织诱导

    The experimental results show that when adopting MS basal medium, adding 2,4-D benefit to induce callus;

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  • 实验结果表明MS为基本培养基,在诱导培养基中加入2,4-D利于愈伤组织诱导

    The experimental results show that when adopting MS basal medium, adding 2,4-D benefit to induce callus;

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