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It includes: mitochondria, endoplasmic reticulum, inside the network devices, lysosomes, microfilaments, microtubules, centriole, etc....

它包括:线粒体、内质网、内网器、溶酶体、微丝、微管、中心粒等。。。。

The series of changes in quantiative and spatial distribution of the three cytoskeleton elements throughout the maturation course of FVA cells was coincided with the process of nucleus eccentricity in position and denucleation, and all of the changes began at the early stage of erythroblast.

一。采用细胞免疫荧光组化方法系统地观察了微丝、微管和中间纤维骨架成分在红系细胞终末分化各阶段的动态变化。

We isolated nine cuticle protein genes, two peptidase genes, and various tubulin isotypes through the EST catalog, and one cuticle protein gene and two protease genes through the microarray analysis.

我们经由EST资料库找到9个表皮蛋白基因,2个胜肽脢基因,和多种的同功型微管蛋白,以及利用微阵列分析找到1个表皮蛋白基因和2个蛋白脢基因。

From the tests,we have obtained some structural variant features related with salt resistance and demonstrated the successful introduction of Rhizophora apicularta DNA into tomato.This thesis contains two parts. In the first part,the morphological and anatomical structures of the leaves were investigated. As to the morphology,some difference between control and transformed tomato were found. The leaf dimensions of the transformed tomato with unextended leaves were smaller than that of control. These structure changes should help to decrease the evaporation of water effectively and release the physiological drought resulted from saline.

本实验分两部分:第一部分、对转化番茄的形态及细胞显微结构进行观察与分析,实验表明转化番茄形态与对照相比有明显的变化,其叶面积变小,叶形收拢,这种结构可有效地减少水分的蒸发,缓解由盐胁产生的生理干旱;组织解剖结构结果显示,耐盐番茄在细胞结构上发生了明显的变异:其气孔器倾向下陷,表皮毛增多,叶脉微管组织不发达,微管束周围出现增多的贮水细胞,叶缘及其它部位表面分化出大型的多细胞分泌型结构,这些结构与转化番茄后代较强的耐盐能力有关。

Methods Immunohistochemistry was used to detect the expression of VEGFR-3,CD31 and lymphatic marker podoplanin in 46 archival surgical specimens of human NSCLC and 8 pulmonary poroma.

结果Podoplanin显示的LVD与CD31显示的血管密度值、VEGFR-3显示的微管密度值不相关(Spearman相关系数0.23,P=0.61;0.09,P=0.84);VEGFR-3阳性管数与CD31阳性管数相关(系数0.80,P=0.031,P.05)。

During the wall thickening, the number of Golgi bodies increased apparently and cytoplasm was filled with Golgi vesicles. Polylamellate structure of the secondary wall appeard, Along with the further development of tracheary elements, the nucleous disappeared and organelles were decreased, while cortical microtubules were arranged neatly against the inner side of plasmalemma.

初生壁与质膜之间有间隔较规律的次生壁突起;中期,线粒体和高尔基体的数量明显增加,细胞质中几乎充满高尔基体及其囊泡,次生壁中微纤丝已成有序排列;晚期,细胞核消失,导管中央形成空腔,细胞器迅速减少,仅观察到少量高尔基体和线粒体,有大量周质微管沿细胞长轴分布,且在次生壁的周围有大量小泡附着,次生壁的分层结构清晰可见。

In addition, we studied the distribution of mitochondria in metaphase Ⅱ rabbit oocytes, zygotes and early embryos by two active mitochondria dyes and revealed the change of active mitochondria during early development of rabbit embryos. We also found that the distribution of microfilaments and microtubules have similar patterns to that of active mitochondria, which is an important basis for further development of animal cloning study using the recipient oocytes derived from rabbit.

此外,我们应用两种线粒体荧光染料研究了日本大耳白兔体内成熟卵母细胞、正常交配后收集的受精卵及早期体外发育胚胎的活性线粒体的位置变化,首次揭示了兔早期胚胎中活性线粒体的变化特征及其与微丝微管变化的相关性,为进一步开展以兔卵母细胞作为核移植受体的动物克隆研究打下了重要的基础。

It possesses a unique mechanism of action as promoters of tubulin aseembly and inhibitors of microtubule disassembly.

它的作用机理独特,通过诱导和促进微管蛋白聚合形成稳定结构,从而抑制微管解聚。

The protein out of which microtubules are made is called tubulin.

构成微管的蛋白质叫做微管蛋白。

Optimal conditions for labeling MFs were tested. Best images were obtained with low fluorescent phalloidin concentration and shorter fixation time. 10nmol/L fluorescent phalloidin was found to be the optimal concentration for MFs localization in BY-2 cells.The distribution of MTs and MFs array in tobacco BY-2 suspension cells during the cell cycle were investigated with confocal microscopy.

采用间接免疫荧光定位及荧光定位技术结合激光共聚焦扫描显微镜等技术,对烟草BY-2悬浮细胞周期中微丝标记的最佳条件、微管列阵与微丝列阵的分布状况进行了研究,结果表明:10nmol/L荧光鬼笔环肽是活体细胞标记微丝的最佳浓度。

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