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The long-term opening of mitochondria permeability transition pore results in the release of cytochrome C, apoptosis inducing factors, Ca2+ and other apoptosis factors into cytoplasm, which can destruct the whole cell structure and function by activating the main member of apoptosis protein family——caspase, or destroying the intranuclear chromoplasm independently, or affecting other protein relying on Ca2+, and finally lead to the formation of apoptotic body.

线粒体是真核生物能量和代谢的中心,也是细胞凋亡信号传导途径中起关键作用的细胞器,越来越多的研究表明,在凋亡信号的刺激下,线粒体发生膨胀,其外膜膜电位降低,外膜破裂后释放出膜间隙的诸多凋亡效应因子,在细胞凋亡中起着主开关的作用。

In my experimentⅠcompare the purposes of different combinations of endoenzyme(MseⅠ-HindⅢ, MseⅠ-PstⅠ, MseⅠ-EcoRⅠ) and find that MseⅠ-HindⅢeasily finds thepolymorphism by primers combinations suiTab for AFLP analysis.And by means of this there aremany polymorphism strips. So the double endoenzyme of AFLP was exercisedfor the analysis of soybean cytoplasmic male sterility.In the cource of my experiment, 64 primerpairs of MseⅠand HindⅢwere exerted to analyse the twe mtDNA pools which are made ofsterilities and holdings and the polymorphisms of sterilities and holdings.

运用扩增片段长度多态性的方法,对独特的杂交大豆试材进行分析研究,通过比较MseⅠ-HindⅢ、MseⅠ-PstⅠ、MseⅠ-EcoRⅠ不同酶切组合的效果,结果表明MseⅠ-HindⅢ较容易找到多态性引物组合,而且具有较高的多态性,本试验选用MseⅠ-HindⅢ进行双酶切大豆线粒体DNA从而完成AFLP的分析工作,试验用64对MseⅠ和HindⅢ引物对两个不育系及保持系材料的线粒体DNA制成的pool进行AFLP标记分析,分析了不育系与保持系之间的多态性; 4。

We determined the complete mitochondrial DNA sequence of Arcyptera coreana (Insecta: Orthoptera: Arcypteridae) and compare it with the other two orthopteran species, Locusta migratoria and Gryllotalpa orientalis.

本文测定和分析了隆额网翅蝗线粒体全序列,并且将其于已经测出全基因组的2种其他直翅目昆虫的mtDNA进行了比较,并联合其他直翅类昆虫的mtDNA进行了线粒体全基因组水平的系统发育分析。获得的主要结果如下: 1。

Mol·L~(-1) individually and also with both heavy metals present. Plasmolysis, concentrated cytoplasm, disappear ance of the cristae of mitochondria, ambiguity of framework and destruction of mitochondria envelope were all symptoms of root cells under Cu stress; hollowing cells was also found in Cd treatment, and there existed some different granule in these hollowing cells.

铜使根细胞产生质壁分离、细胞质浓缩、部分细胞空泡化,使线粒体脊突消失、结构模糊、外膜破坏;镉使根细胞空泡化,并在部分空泡化的细胞里产生大小不等的颗粒状物;铜、镉交互污染使根细胞受害程度加深,并兼有两者的受害症状特征:线粒体结构彻底破坏、空泡化细胞里的颗粒物更大电子密度更高、质壁分离现象更普遍、质膜上的颗粒物沉淀更大。

Using the intact G1-nuclei prepared from an isogenic yeast strain lacking mitochondrial DNA , we demonstrated that the DNA synthesis observed within the first 10-20 min was largely due to mitochondrial DNA synthesis, whereas nuclear DNA synthesis did not begin until after a 10-20 min lag period.

利用从缺少线粒体DNA的菌株中制备的完整G1期细胞核,证明了最初10-20min的滞后期内的DNA合成主要是由线粒体DNA合成造成的,而核DNA合成是在经过10-20 min后才开始。

Light microscope and transmission electron microscopy showed that SMMC-7721 cells induced by SAHA had undergone the restorational alteration in morphology and ultrastructure, which were different from those of nontreated cells but were similar to those of normal cells, and the changes were as follows: the cells turned to be flat and spread; the nucleo-cytoplasmic ratio lessened and nuclear shape became rather regular; the number of nucleolus reduced and its volume lessened; euchromatin increased while heterochromatin decreased in nucleus; in the cytoplasm, mitochondria grew in number with relatively consistent structure and well-developed mitochondria cristae; Golgi complex turned to be well-developed and typical; rough endoplasmic reticulum increased. Immunocytochemistry assay showed that the expression of AFP and PCNA were declined significantly. FCM analysis showed SAHA could arrest SMMC-7721 cells in G0/G1 phase, with an accumulation of the cells in G0/G1 phase while a decrease of cells in S phase. Semi-quantitative RT-PCR detection revealed that the expression of p21WAFl mRNA was upregulated remarkably in the cells treated with SAHA.

结果:倒置显微镜和透射电镜观察显示,经SAHA处理的细胞增殖速度显著减慢,细胞体积增大,细胞核较小,形状较为规则,核仁数量减少、体积变小,核内常染色质增多而异染色质减少,核质比例减小,细胞质内线粒体数量增多、线粒体嵴发达,高尔基体较为典型,粗糙型内质网增多,呈现出与正常上皮细胞相似的形态变化;MTT比色法测定结果显示不同浓度(2.5、5.0、7.5、10.0uM)SAHA对SMMC-7721细胞的增殖均有抑制作用,并有明显的剂量依赖和时间依赖关系;免疫细胞化学检测显示SAHA能显著降低PCNA和AFP在SMMC-7721细胞中的表达;流式细胞仪检测结果显示,SMMC-7721细胞经SAHA处理后,G0/G1期细胞明显增加,S期细胞则明显减少,细胞被阻滞于G0/G1期;RT-PCR检测结果表明,SAHA作用12h后SMMC-7721细胞中p21WAF1 mRNA的表达即有增加,24h后更为明显。

Usually, anti-apoptotic protein is insulated in organella, restraining the release of pro-apoptotic factor and controlling cell apoptosis. however, interacting with pro-apoptotic protein, it can not restrain apoptosis, induce the loss of mitochondrial function, accelerate the release of pro-apoptotic factor and result in apoptosis.

抑凋亡蛋白平时被隔离在线粒体等细胞器内抑制促凋亡因子的释放,具有抑制细胞凋亡的功能,但一旦与激活的促凋亡蛋白发生相互作用后,便丧失了对细胞凋亡的抑制作用,造成线粒体等细胞器的功能丧失和细胞器内促凋亡因子的释放,导致细胞凋亡。

Anti-apoptotic and pro-apoptotic factors have synergistic effect and play a switch role. Usually, anti-apoptotic protein is insulated in organella, restraining the release of pro-apoptotic factor and controlling cell apoptosis.

抑凋亡蛋白平时被隔离在线粒体等细胞器内抑制促凋亡因子的释放,具有抑制细胞凋亡的功能,但一旦与激活的促凋亡蛋白发生相互作用后,便丧失了对细胞凋亡的抑制作用,造成线粒体等细胞器的功能丧失和细胞器内促凋亡因子的释放,导致细胞凋亡。

The size of follicle begin primordial follicle to tertiary follicle(1.5~3mm).The number of mitochondrion increased,and the cristae increased.Gogi body change to type,cortical granule increased,and moved behind cytolemma.The proportion of small,middle and large follicles on ovary were 92.51%(92.51±5.87),4.60%(4.60±4.91) and 2.88%(2.88±2.22) respectively.

卵泡在发育过程中,卵泡细胞形成的突起与卵母细胞始终保持密切的联系:卵母细胞从原始卵泡到直径1.5~3mm的三级卵泡,细胞质中线粒体数量由少到多,线粒体内的嵴不断增加,高尔基体由不典型到变成典型,皮质颗粒由开始形成到形成较多的皮质颗粒,并逐渐地迁移到卵母细胞膜下。

Dense cytoplasm with abundant mitochondria, endoplasmic reticulums, multivesicular bodies, vesicles and plastids were observed in normal light intensity.

在正常光照下的伴胞具有致密的细胞质,内含丰富的线粒体、内质网、多泡体、囊泡和质体,而弱光下的伴胞明显液泡化,同时含有少量的线粒体和内质网。

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