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核染色细胞

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RESULTS: There was plentiful COX2 protein in the cortex, the hippocampus, the dentate gyrus, the supraoptic nucleus, the amygdaloid nucleus, cerebellum and brain stem, and so on.

结果:在正常成年大鼠脑内COX2蛋白主要表达于皮层、海马、齿状回、视上核、杏仁核、小脑和脑干等部位,阳性细胞主要为神经元,神经胶质细胞染色很少。

RESULTS: There was plentiful COX2 protein in the cortex, the hippocampus, the dentate gyrus, the supraoptic nucleus, the amygdaloid nucleus, cerebellum and brain stem, and so on. The COX2 immunopositive cells were mainly neurons, and a few were glial cells.

结果:在正常成年大鼠脑内COX2蛋白主要表达于皮层、海马、齿状回、视上核、杏仁核、小脑和脑干等部位,阳性细胞主要为神经元,神经胶质细胞染色很少。

We also confirmed in this paper that it is injected somatic cells but not broken cytoplasm formed multi blastomere through mitosis in the reconstructed embryos.

在本实验中还通过用DNA染料(Hoechst-33342)对核移植体进行染色的方法,对融合后成纤维细胞在核移植体内不同时间的运行及发育模式进行了观察,确认了是成纤维细胞经有丝分裂形成多个卵裂球而不是由于细胞质碎裂形成的两个或多个碎块。

Due to the breakthrough of stained technology in 1970s, the band-pattern of chromosome provides material visual information for cytogeneticist, then analyses the composition of genome in a cell and measures the features of the equipments for karyotyping.In order to meet the demands of clinical hospital, a chromosome analysis system based on PC is developed.

由于70年代标本染色技术的突破(取代了此前的均匀染色方法,产生了染色体的带型特征),染色体的带型模式为细胞遗传学家提供了实质性的视觉信息,从而可以进一步分析细胞的基因组的合成以及进行自动核型分类仪器中的特征测量。

The amount of vimentin IF per cell was higher than those of tubulin and F-actin at 12-24h of culture, but it broken down and decreased steadily when the cells became differentiated into late erythroblast at 36-48h of culture, thus facilitated the eccentric nucleation which we regard it as the initial step of denucleation. Both of the fluorescence intensity of tubulin and actin exhibited a significant rise and aggregated between the extruding nucleus and incipient reticulocyte before and during denucleation, and finally play a role in the commitent to ennucleation, the second phase of denucleation.

在培养24小时前,每个细胞中波形纤维含量均高于同期微丝和微管蛋白含量,但在培养24-36小时的晚幼红细胞阶段,波形纤维蛋白降减和解聚,为核偏位创造了条件,这是排核的第一阶段,而随后微丝和微管蛋白的荧光染色强度则有所增加,并逐渐聚集在外排中的核与预期形成网织红细胞之间的缢痕区,在将细胞核排出的排核第二阶段起主要作用。

Cases of the abnormal sex differentiated diseases in children were presented. Among them, there were 4 cases of Turner's syndrome, 1 Klinefelter's syndrome, 9 female pseudohermaphroditism, 2 male pseudohermaphroditism, and 4 true hermaphroditism.

本文报道小儿性分化异常疾病20例(包括先天性卵巢发育不全综合征4例、先天性睾丸发育不全综合征1例、女性假两性畸型9例、男性假两性畸型2例、真两性畸型4例),对上述病例进行了细胞染色体核型分析,同时作了口腔上皮细胞性染色质、中性粒细胞核鼓植体及尿17酮类固醇、17羟类固醇的检查。

RESULTS: There were many vacuoles and cracks in the cells, with heterochromatin margination, nuclear pycnosis and nuclear fragmentation. The high intensity pulsed electric fields caused damage in K562 cells, and the apoptotic percentage went up with the increase in frequency and intensity of PEF.

结果:经过高电压脉冲电场处理后的K562细胞,胞内出现大量空泡及裂隙,核内染色质向核周边聚集形成凋亡小体,呈典型细胞凋亡形态学改变;K562癌细胞的凋亡比例随着脉冲个数和电场强度的增加而增加。

Results:17 rats were confirmed successful transplantation by MRI,the capacity of the tumor was 88.40±7.62mm3 on 8th day, 986.80±114.46mm3 on 16th day,the volume growth was 8-12 folds;on 8th day following transplantation,the tumor tissue was gray in color with fish homogen state without interior necrosis, the tumor cells were nest-distributed by HE staining,large dense staining of nucleus with manifest heteromorphism,tumor microvessel count increased by immunohistochemistry with buffy yellow staining, VEGF high expressed in the tumor cells with buffy yellow granule shape.

结果:17只大鼠经MRI检查证实均种植成功,肿瘤体积第8天为88.40±7.62mm3,第16天为986.80±114.46mm3,体积增长8-12倍之间;种植第8天,肿瘤组织呈灰白色、鱼肉均质状,内部未见坏死,HE染色肿瘤细胞呈巢状分布,胞核大浓染,异型性明显;免疫组织化学示肿瘤微血管数目较多,呈棕黄色染色,肿瘤细胞VEGF高表达,呈棕黄色细颗粒状。

Methods Fourteen mutated vpr fragments were selected from patients with HIV. Both eukaryotic expression vector pcDNA3.1 and PCR products were purified, double-cut by Hind Ⅲ and BamH Ⅰ, and the cut products were legated and transformed into competent cells JM109. The 14 reconstructed plasmids were transfected into Hela cells. Cells with pcDNA vpr-wt, pcDNA vpr-Fs and pcDNA3.1 blank cells, and without pcDNA3.1 cell were established.

以14个带有HIV-1vpr基因片段的PcD-NA3.1真核表达载体构建重组质粒,将其转染Hela细胞,并设立保守株vpr基因转染细胞、突变株vpr-FS基因转染细胞、空载体转染细胞和未转染细胞作为对照,经逆转录多聚酶链式反应检测目的基因转染成功后,Pi染色,用流式细胞仪检测被转染细胞的细胞周期分布和细胞凋亡率。

Methods 14 mutanted vpr fragments selected from Chines patients with HIV. Both eukaryotic expression vector pcDNA3.1 and PCR products purified , double-cut by HindⅢ and BamH and the cut products legated and were into competent cells JM109. The 14 reconstructed plasmids electronically transfected into hela cells, and established cells with pcDNA vprwt 、pcDNA vpr-Fs and pcDNA3.1 blank cells, and without pcDNA3.1 cell.

将14个带有HIV-1 vpr基因片段的pcDNA3.1真核表达载体构建重组质粒,将其转染Hela细胞,并设立保守株vp r基因转染细胞、突变株 vpr-FS基因转染细胞、空载体转染细胞和未转染细胞作为对照,经RT-PCR检测目的基因转染成功后,经Pi染色用流式细胞仪检测被转染细胞的细胞周期分布和细胞凋亡率。

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