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The results by invert embedding TEM showed that higher invasive CCL229cells had vast of ER,which distributed throughout cytosol especially largeamount of vesicle-like and flatten cisternal rER in pseudopodia or cell processesand membranous flow-like structure from perinuclear region to pseudopodia,and less Golgi complex.

倒置包埋法常规透射电镜对人大肠癌细胞的超微结构观察结果显示,高侵袭力的CCL229细胞中内质网数量较多并呈全细胞分布,尤其在细胞伸出的众多伪足中含有丰富的小泡状和扁平囊样粗面ER结构,而且观察到由小泡形成的&膜流样&结构从核周一直深入到伪足中,但细胞中高尔基器少见。

METHOD:SD rat aortic tissue was planted with the adherent method of tissue explants. The cellular morphology was observed by inverted phase contrast microscope and the nucleus and cytoplasm were observed after haematoxylin and eosinstaining.

运用组织块贴壁法进行SD大鼠胸主动脉平滑肌细胞培养,并用倒置相差显微镜观察、HE染色后形态学观察以及用免疫组化对培养细胞进行鉴定。

The cells were identified by invert phase contrast microscopy and alkaline phosphatase staining and mineralized nodules staining.The activity distribution of osteoblasts was determined by microtitration during a culture cycle.

通过倒置相差显微镜观察,并用碱性磷酸酶和矿化结节染色鉴定,利用微量滴定法测定一个培养周期的成骨细胞活性分布,探讨一种经济、高效的原代成骨细胞培养方法。

Methods: The inhibitation of HL-60 cells by Rapamycin was measured by MTT assay. Morphic change of the apoptosis of HL-60 cells was observed by inverted microscope and light microscope, trapezoid straps by DNA agarose gel electrophoresis, and apoptosis rate by flow cytometry. Western-blot analysis was performed to detect the expression of Bax and Bcl-2 proteins after rapamycin treatment.

用MTT比色法测定雷帕霉素对HL-60细胞增殖的影响;用倒置显微镜和荧光显微镜观测细胞凋亡的形态学改变;DNA琼脂糖凝胶电泳观测凋亡的梯形条带;流式细胞仪检测细胞凋亡率;Western-blot检测HL-60细胞经雷帕霉素处理后,Bax、Bcl-2蛋白的表达情况。

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。

The biological features of hBMSCs and cryogentic storaged cells were analyzed.hBMSCs memberane antigens were identified by immunofluorescence staining.The potential osteogenous differentiation of hBMSCs was evaluated by the osteogeneic inducer kit.

倒置光学显微镜下观察细胞形态及生长情况,细胞计数法绘制细胞生长曲线,并分析冻存细胞复苏后的生长特性,免疫荧光染色测定hBMSCs表面标志,成骨诱导试剂盒检测hBMSCs向成骨分化的潜能。

The function of bone resorption by MGC was examined with coculture of bone slice and MGC. The resorption lacunae were examined with a scanning electron microscope. The activity of acid phosphatase in MGC was observed by Gomori stain. Results: MGCs showed multinuclei (more than 20 nuclei), irriegular peripheral cytoplasm with pseudopodial projections, vacuoles were seen in the cytoplasm.

用倒置相差显微镜观察体外培养的多核巨细胞的一般形态及降钙素对它的影响;用骨片与多核巨细胞共同培养法观察多核巨细胞的体外骨吸收功能,用扫描电镜观察骨吸收陷窝,Gomori染色观察多核巨细胞的酸性磷酸酶活性。

Pyriformis cells cultivated in liquid complex culture media containing 0, 0.05, 0.25, 0.5, 2.5, and 5 mg/mL of melamine were plotted by recording the number of cells present in the culture medium during the course of a 52-hour cell growth experiment, with a strictly controlled time interval of 4 hours.

本实验利用倒置光学(来源:A83B38f6C论文网www.abclunwen.com)显微镜下血球计数板计数法进行细胞计数,每两次细胞计数之间的时间间隔为4小时。

Methods:Single guinea pig ventricular myocytes were obtained by retrogradely perfusing with collagenase through the aorta.

用主动脉逆向灌流法酶解分离得到单个豚鼠心室肌细胞,在倒置显微镜下,选择质膜完整、横纹清晰的心室肌细胞,利用膜片钳技术经过封接、破膜、电容及串连电阻的补偿形成膜片钳全细胞记录状态。

Methods : MTr assay was used to examine the effect of Sorbaria sorbifolia on the proliferation of HepG-2 cell and flow cytometry was used for the cell cycle distribution.

采用MTT比色法观察珍珠梅提取物抑制肝癌HepG-2细胞增殖;采用流式细胞仪检测其对HepG-2细胞周期分布的影响,同时结合倒置显微镜、HE染色、透射电镜及免疫细胞化学方法检测凋亡相关基因bcl-2、p53的蛋白表达,观察其诱导肝癌HepG-2细胞凋亡的作用。

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