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The invention discloses a connecting city white duck blastodisk fiber cell system with connecting city white duck embryo as material with preservation number at CGMCC No.1877 in cellular biology domain, which is characterized by the following: the fiber cell does not possess epithelial cell with high purity; the quality of freezing cell is stable; the active ratio can reach between 93.5% and 96.8%; the passage growth is stable and fit for big scale culture.

本发明利用连城白鸭胚胎作为材料,进行初代培养、传代培养及细胞冻存等研究。最终获得高活率、高纯度的连城白鸭胚成纤维细胞系,其保藏编号为CGMCC No.1877属于细胞生物学领域。本发明培养的成纤维细胞无上皮细胞等,细胞纯度高;冻存后细胞质量稳定,活率可达到并维持在93.5%~96.8%之间,传代生长稳定,适合大规模培养。

Compared with the corresponding BEAS-2B cells, the shapes of cells and nuclears, the shapes and quantity of cell organs were not significantly changed in the 1st, 2nd, 5th passage BEAS-2BNNK cells. The 10th, 15th passage BEAS-2BNNK cells, which had swelled cell and cell organs and abnormal nuclear and enlarged the nucleoli gradually and increased the quantity of the cell organs and activated their function, showed the characteristic of transformation cells. The 20th, 25th passage BEAS- 2BNNKcells, which had obvious aberration of the cell and nucleoli and had cataclasm of nucleoli and decreased cell organs, showed the characteristic of tumor cells.

与BEAS-2B相比较BEAS-2BNNK第1、2、5代细胞及胞核形态、细胞器形态及数量无明显差别;第10、15代细胞出现肿胀,细胞核逐渐变形,出现核畸形,核仁明显增大,边集,细胞器肿胀,数量明显增多,功能活跃具明显的转化细胞特征;第20、25代细胞及胞核明显畸变,出现明显的核碎裂及多个核仁,细胞器明显减少,具明显的肿瘤细胞特征。

Results 2 ClAdo and 2 CldAdo had different cytotoxicities on the cells, while 2' dAdo had no cytotoxicity on the cells. 2 CldAdo blocked the cell growth at the phase of S and G2/M, while 2 ClAdo at the phase of G0/G1. 2 CldAdo mainly induced cell necrosis, while 2 ClAdo induced both cell necrosis and apoptosis. Down regulated Bcl 2 expression and up regulated p53 and Bax expression were associated with 2 ClAdo, while 2 CldAdo down regulated Bcl 2 expression and up regulated mildly p53 expression without any effect on Bax expression.

结果 2 ClAdo、2 CldAdo对所研究的细胞均有程度不等的毒性;2' dAdo对各细胞生长、增殖均无明显抑制(c=100 μmol/L即30 μg/mL内);2 CldAdo明显阻断细胞于S、G2/M期,2 ClAdo阻断细胞于G0/G1期;2 CldAdo 致细胞坏死为主,2 ClAdo 既致细胞坏死又诱导凋亡;2 ClAdo 下调Bcl 2,上调P53、Bax蛋白表达;2 CldAdo小幅上调P53、小幅下调Bcl 2,不影响Bax蛋白表达。

These ingredients includes epidermal growth factor, hepatocyte growth factor, dimethyl sulfoxide, phenobarbital sodium and all trans-retinoic acid. We isolate and culture primary 10-weeks-old human fetal hepatocytes, observe hepatocytes form and its function markers. Inoculate hepatocytes with HBV Dane particles to observe if HBV susceptibility of fetal hepatocytes can be induced in vitro. To detect HBV covalently closed circular DNA within hepatocytes, we improve the existent PCR method.

基于上述假设,我们设计了10种培养条件,在自行设计的无血清培养基中添加不同的细胞分化诱导物,包括表皮生长因子、肝细胞生长因子、二甲基亚砜、苯巴比妥钠、全反式维甲酸等,分离孕10周龄人胎肝细胞进行原代培养,观测肝细胞形态及功能指标变化,并定时给予HBV感染,观察能否在体外诱导胎肝细胞出现HBV易感性;为检测肝细胞内HBV共价闭合环状DNA(covalently closed circular DNA,cccDNA),我们改进了现有的PCR检测法。

To understand the degeneration of unfertilized aposporous embryo sac in an aposporous species Pennisetum squamulatum, the central cell in the unfertilized embryo sac was characterized ultrastructurally.

为理解植物无孢子生殖胚囊未受精条件下的退化,对无孢子生殖植物非洲狼尾草未受精成熟胚囊中央细胞退化做了细胞形态学研究。

MUC2 apomucin and its mRNA were mainly located in the peri-and supranuclear area of goblet cells of duodenum and column,but no signal in the columnar-type cells.

结果发现,胃粘膜中无MUC2和MUC3基因产物的表达,MUC2核粘蛋白及mRNA主要存在十二指肠和结肠杯状细胞周及核上,柱状细胞中无表达。

Of CBMC can be purified by Mini-MACS as CD34〓 stem cells. B. The number of CD34〓 stem cells can expand to 40.24±9. 86 fold after 14 days. C. No matter in the expression of CD1a, CD80, CD86, and HLA-DR, or in the function of stimulating xenogenous lymphocyte proliferation, there was no difference between CD34+ stem cell DCs or monocyte DCs. D. The percentage of CD3〓CD56〓 cells is the same in CIK cells co-culture with DCs transfected with SKOV3 RNA, CIK cells co-culture with DCs, and CIK cells. E. The expansion rate of CIK cells can be accelerated by co-culturing with loaded or unloaded DCs. However, the expansion rate between loaded or unloaded group is the same. F. The strongest cytotoxicity against SKOV3 cell line was achieved by CIK cells co-cultured with DCs loaded with SKOV3 RNA.

结果:1、Mini-MACS分选系统可自CBMC中提取0.78±0.31%的CD34〓细胞;2、体外培养14天后可获得原始CD34〓细胞量40.24±9.86倍的细胞;3、不论在CD1a、CD80、CD86及HLA-DR的表达上,或是刺激异体淋巴细胞增生的功能上,脐带血CD34〓细胞与单核细胞来源的DC都没有差别;4、CIK细胞中CD3〓CD56〓双阳性的表达率在与RNA转染DC共培养的CIK细胞组、与DC共培养的CIK细胞组及单纯CIK细胞组3组间比较无差异;5、脐带血CIK细胞增殖显著,培养14天时可扩增18.18±5.59倍,培养21天时可扩增35.02±6.30倍;5、与未转染或转染DC共培养的CIK细胞在培养第14天后增殖速率大于单纯CIK细胞。

The cells survival rates of every group were determined by MTT technique.Results The tumor cells without any anti-glioma factor treatment were growing better and no change was observed in morphology.After 2-3 days,cell axons disappeared,cell bodies crimpled,nucleoli crinkled and cracked in each treated group.

结果 未加任何抗癌因子处理的C6细胞组肿瘤细胞生长旺盛,细胞形态无明显改变;各处理组的肿瘤细胞2~3天后开始逐渐出现细胞突触消失,细胞变圆,胞体皱缩,核仁固缩、裂解、甚至消失,继而逐渐死亡。

In vivo, composition E markedly protected mice from lethal challenge by heat-killed E. coli and heat-killed S. aureus. Conclusions:(1) Targeting on PGN, CpG DNA and lipid A, we successfully established the platform to screen anti-inflammatory traditional Chinese medicine using biosensor technology which is highly effective, objective and feasible.

该组分经MTT法测定对小鼠RAW264.7细胞活力无影响(≤400μg/ml),经CCK-8法测定也对小鼠RAW264.7细胞活力无影响(≤800μg/ml);对PGN、CpG DNA及LPS刺激小鼠RAW264.7细胞分泌TNF-α有显著的抑制作用,并呈现良好的剂量-效应关系;对致死剂量的热灭活大肠杆菌和热灭活金黄色葡萄球菌攻击小鼠有显著的保护作用。

The results showed that the plant had the character of damp-inhabiting, the cutical on the epidermis of stem and leaf is rather thin but without wax-layer, its stomata protrude clearly on the lower surface of leaf, the rate of palisade parenchyma and spongy parenchyma is rather low and the cortex is well developed in root.

结果表明蓝靛果具有明显的湿生特征:茎、叶表皮的角质层薄,无蜡被;叶片上表皮细胞甚大,无气孔,下表皮细胞小,气孔明显突起;叶脉导管直径小,壁薄;叶肉栅栏组织/海绵组织小;根的皮层发达,富细胞间隙。

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