They were induced to small calli in the medium.
原生质体在培养基中诱导出小愈伤组织。
The calli produced buds on differentiation medium.
愈伤组织在分化培养基上产生幼芽。
The calli were placed on MS medium for proliferation.
然后转入固体培养基中增殖。
This is the first report of obtaining bergenin from calli of Ardisia spp.
本文首次报道从紫金牛属植物的愈伤组织中检出岩白菜素。
The most of calli grow well and the callus induction frequency was 96.8%.
其愈伤组织绝大多数生长良好，出愈率达96.8%。
GUS assay indicated that foreign gene had expressed in maize cell and calli.
GUS染色证明外源目的基因在玉米细胞和组织中得到了表达。
In Citrus, the embryogenic calli consisted of embryogenic and non-embryogenic cells.
长期继代培养的柑橘胚性愈伤组织由胚性细胞和非胚性细胞组成。
The results showed that leaf explant calli were originated from succulent leaf cells.
结果表明：叶片愈伤组织起源于叶肉细胞；
And the contents of total alkaloid in adventitious roots is higher than that in calli and buds.
其中不定根中的总生物碱含量高于愈伤组织和不定芽丛。
Many embryogenic calli were produced by subculture of calli induced from mature embryo of rice.
从水稻成熟胚诱导出的愈伤组织经继代培养后可以产生大量的胚性愈伤组织。
Media had obvious effect on calli induction and differentiation. MS medium was better than DCR medium.
培养基类型对愈伤组织的诱导和分化有明显影响，MS培养基优于DCR培养基。
The LEAFY gene was also introduced into cells of sugarcane calli using PDS-1000 he particle bombardment.
本研究同时以甘蔗心叶愈伤组织为受体，通过PDS- 1000氦气基因枪轰击，将LEAFY基因转入甘蔗细胞。
The CC medium was an efficient selectable medium for screening hygromycin resistant calli after co cultivation.
以CC培养基作为共培养后抗性愈伤筛选的基本培养基有利于抗性愈伤组织的筛选培养。
Cell cycle analysis can provide reference for researching the physical and chemical mutagenesis to citrus calli.
细胞周期分析可为研究柑橘愈伤组织理化诱变提供依据。
Enzyme activity of GUS and NOS assay demonstrated that foreign genes expressed in the transformed plants and calli.
GUS活性检测和胭脂碱分析表明，外源基因在转化细胞内得到稳定表达。
But all the calli induced by immature embryos did not differentiate the embryoids through solid and liquid subculture.
但幼胚诱导的愈伤组织经固体继代培养和液体悬浮培养后，都没有胚状体的分化。
Predifferentiation showed that ABA was effective to increase the frequency of regeneration of protoplast-derived calli.
预分化实验表明：ABA能有效地提高原生质体愈伤组织的再生能力。
The green shoot-bud regeneration rates of calli were affected by combinations of different auxins in regeneration medium.
分化培养基上不同激素配比也影响其绿苗再生率。
By this token, induction and subculture of embryonic calli should be related with cooperative effects among different hormones.
由此看来，胚性愈伤组织的诱导和保持，可能还与各种激素的协同作用有关。
Calli were induced from cotyledons, hypocotyls, and taproot cambium of Daucus carrot. and cell suspension lines were established.
分别以胡萝卜子叶、下胚轴和直根形成层为外植体诱导出愈伤组织，并建立细胞悬浮系。
By particle bombardment method, 167 regenerated plantlets were gained from 1160 calli, and the transformation frequency was 17.4%.
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%。
Calli of an indica rice cultivar Qiuguiai 11 were used as material for a further study on the effects of copper in calli cultures.
以籼稻栽培品种秋桂矮11的愈伤组织为材料，对铜元素的作用作了进一步的研究。
Plantlets were subjected to RAPD analysis, and the result of RAPD showed that regenerants from calli had a higher genetic variation.
再生的植株经rapd分析表明，经过愈伤组织再生的植株遗传变异性较高。
The results showed that the levels of endogenous phytohormones in embryogenic calli were higher than those in non-embryogenic calli.
结果表明，龙眼胚性愈伤组织中内源激素含量比非胚性愈伤组织高；
Adding sorbitol to the subculture medium could improve the growing state of the calli and decrease the percentage of Browning calli.
在继代培养基中添加山梨醇能改善愈伤组织的生长状态，降低愈伤组织的褐化。
Salidroside accumulation of calli inducted from leaves of female and male had more significant difference, and male was more than female.
由雌、雄植株叶片诱导的愈伤组织红景天甙含量有极显著差异，由雄株叶片诱导的愈伤组织红景天甙含量高于雌株。
We selected PC resistant rice calli, which were derived from anther culture, using one of the PCs, bispyribac-sodium (BS), as a selection agent.
我们以双草醚钠这种嘧啶羧酸类除草剂为筛选剂，对来源于花药培养的愈伤组织进行筛选。
High concentration of sucrose is favourable for the male nuclear development. There were 8 chromosome in the calli cells, proving to be monoploid.
高浓度蔗糖有利于雄核发育，愈伤组织染色体数8，证明其为单倍体。
Using embryogenic calli from young embryos as explants, bean chitinase gene was transferred into spring wheat plants by microprojectile bombardment.
利用基因枪法，以菜豆几丁质酶基因转化小麦幼胚愈伤组织。
Using embryogenic calli from young embryos as explants, bean chitinase gene was transferred into spring wheat plants by microprojectile bombardment.
利用基因枪法，以菜豆几丁质酶基因转化小麦幼胚愈伤组织。
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