再生植株农艺性状与对照相似。
The agronomic traits of regenerants were similar to the contrasts.
再生植株根系发达，叶片具三叶特征。
The regenerated plants were trifoliate with well developed root systems.
再生植株的移栽成活率达90%以上。
A survival rate of transplanted plantlets of regeneration was more than 90%.
通过控制光温条件，可迅速再生植株。
Numerous plantlets were able to be produced by culture under regulated temperature and light conditions.
再生植株的产生主要是通过直接器官发生途径。
The plant regeneration occurred mainly by means of direct organogenesis.
这是迄今第一个由籼稻原生质体再生植株的报道。
This is the first report of plant regeneration from the protoplast culture of an indica rice.
汕优6号再生植株的诱导能力大于台中育39。
The inducibility of Shah You-6 was higher than that of Tai Zhong Yu-39.
融合产物经过4 - 5个月的培养获得再生植株。
The fusion products regenerated into plantlets within 4-5 months.
两个胡萝卜和两个烟草冠瘿株系分别得到再生植株。
Plantlets have been induced from two carrot crown gall strains and two tobacco crown gall strains.
本试验摸索了适宜冬枣叶片再生植株移栽的环境条件。
The experiment studied the suitable transplant conditions of tube-plants.
成熟培养能促进体胚的生长发育、提高再生植株的数量。
Maturation culture could accelerate somatic embryo developing and enhance the amount of regeneration plant.
以悬浮培养的水稻细胞过滤出的单细胞成功地再生植株。
Regenerated plantlets were obtained from the single cells filtering through the mesh.
筛选得到了多个抗(耐)毒素细胞系和分化的再生植株。
A plenty of cell lines resistant (or tolerant) to DON toxin were isolated and many plants regenerated from them.
水稻组织再生植株的诱导能力因种类、器官、培养基等而异。
The inducibility of tissues of rice to regenerate plant lets varied according to the species, organs or media.
茎尖和花序分别以器官发生和体细胞胚胎发生方式再生植株。
Shoot apices and inflorescence respectively regeneratebamboo plantlets by means of organogenesis and embryogenesis.
芦笋的花药、花粉、茎尖及原生质体经离体培养均可再生植株。
The anther, pollen, stem point and bioplast cultured in vitro can be plant.
本试验用外源植物DNA处理水稻离体胚，并获取胚的再生植株。
Rice plants can be regenerated from the in vitro embryo treated by exogenous plant DNA in the experiment.
胚胎发生能力和再生植株转化率是游离小孢子培养技术的关键问题。
Improving microspores embryogenic ability and plantlet regeneration ability from microspore-derived embryos is the key of isolated microspores culture technique.
利用高压纸电泳法对毛状根和再生植株进行T-DNA转化的检测。
The transformation of Ri T DNA was examined through high voltage paper electrophoresis.
对取自烟草变异株的腋芽进行扦插和叶片组织培养，均已成功地获得再生植株。
Through cuttage of axillary buds and leaf tissue culture, numerous regenerated plantlets had been produced and were transplanted in the field.
通过诱导愈伤组织再分化和直接诱导不定芽这两种途径获得了石竹的再生植株。
The regenerated plantlets in Dianthus chinensis were obtained by two methods: through the redifferentiation of the callus and the adventitious buds induced directly from the explant.
不同激素配比的分化培养基在诱使再生植株染色体倍性变异方面存在着明显差异。
The differentiation media with different rates of growth regulators demonstrated distinct difference in inducing ploidy variation for regenerated plants.
以红姜茎尖薄片胚性愈伤组织为材料建立了胚性细胞悬浮系，并获得了再生植株。
Regenerated plantlets were obtained in embryogenic cell suspension culture from embryogenic callus of stem slice in Hedychium coccineum Buch-Ham.
通过测量气孔保卫细胞长度来评估再生植株的染色体倍性是一种简单可行的方法。
The method for measurement of the length of stoma guard cell was proved to be a simple way of estimating ploidy of the regenerated plants.
这种变异在植物组织培养后的再生植株中常表现得非常广泛，而且变异频率非常高。
The variation is quite common among regenerated plants after tissue culture, and the frequency of mutation is very high.
同时对花药壁、植物激素在花粉粒发育中的作用及再生植株染色体倍性问题进行研究。
In the meantime, we studied the action of anther wall, plant hormone in developing of the pollen, and chromosome multiple of regenerate plantlets.
通过基因枪转化法轰击1160块的愈伤组织得到167株再生植株，转化率17.4%。
By particle bombardment method, 167 regenerated plantlets were gained from 1160 calli, and the transformation frequency was 17.4%.
通过农杆菌介导，采用叶盘法将豌豆凝集素基因转化单倍体烟草，获得了转基因再生植株。
The pea lectin gene was transformed into the haploid tobacco via Agrobacterium mediation using leaf disc method and the regenerated tobacco plants were obtained.
将海岛棉茎尖分生组织经过3～6周的诱导、继代培养生长后，可以形成足够量的再生植株。
Sufficient plantlets of regeneration were produced within 3~6 weeks induced and culture from apical meristems.
将海岛棉茎尖分生组织经过3～6周的诱导、继代培养生长后，可以形成足够量的再生植株。
Sufficient plantlets of regeneration were produced within 3~6 weeks induced and culture from apical meristems.
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