生长曲线

Phosphorus content in accordance with the abscissa, the ordinate physiological parameters for growth curve for result analysis.

按照以磷含量为横坐标，各项生理参数为纵坐标绘制生长曲线，进行结果分析。

K562 cell cultivated in suspension and adhesively cultivated with MSC were collected respectively and cell proliferation curves were drawn; the cell cycle was determined by flow cytometry; the effect of chemotherapy on cellular viability and apoptosis of...

对悬浮培养和与MSC黏附培养的K562细胞绘制细胞生长曲线；用流式细胞术测定细胞周期并观察化学药物对细胞存活率和凋亡的影响；用RT-PCR技术检测MDR1基因表达。

K562 cell cultivated in suspension and adhesively cultivated with msc were collected respectively and cell proliferation curves were drawn; the cell cycle was determined by flow cytometry; the effect of chemotherapy on cellular viability and apoptosis of k562 cell was investigated,the mdr1 gene expression was determined by rt-pcr.

对悬浮培养和与msc黏附培养的k562细胞绘制细胞生长曲线；用流式细胞术测定细胞周期并观察化学药物对细胞存活率和凋亡的影响；用rt-pcr技术检测mdr1基因表达。

K562 cell cultivated in suspension and adhesively cultivated with MSC were collected respectively and cell proliferation curves were drawn; the cell cycle was determined by flow cytometry; the effect of chemotherapy on cellular viability and apoptosis of K562 cell was investigated, the MDR1 gene expression was determined by RT-PCR.

叶悬浮培养和与MSC黏附培养的K562细胞绘制细胞生长曲线；用流式细胞术测定细胞周期并观察化学药物对细胞存活率和凋亡的影响；用RT-PCR技术检测MDR1基因表达。

Methods The total proteins of untreated and INH-treated mc^2 155 cells were separated by ampholyte pH gradient-based two-dimensional gel electrophoresis (2-DE). Tire differential expression proteins were analyzed by using image analysis software. Results Proteins of control group arid INH-treated group contained 159 and 221 protein spots, respectively.

观察不同浓度的异烟肼处理前后耻垢分枝杆菌生长曲线，确定药物处理SM细胞的最佳时间和浓度，并提取在最佳处理时间和浓度条件下的SM细胞总蛋白，采用载体两性电解质pH梯度双向凝胶电泳技术分离异烟肼处理前后耻垢分枝杆菌mc^2 155细胞的总蛋白质，用PDuest 7.3.1图像分析软件比较分析，以识别差异表达的蛋白质。

The morphology and structure of reconstructed tissue was detected by microscope and scanning electron microscope.Results:(1) Compared with the control group, the cellular proportion of laminin group increased in 62 ~M phase, and decreased in Go~Gi phase significantly. As shown by the microscope, the cells of control group were in low density. The cells in mass connected tightly. The microfilament appeared reticular formation. The nucleus were the same in size. The cells of laminin group were in high density and put out so many lamellipodia, filopodia, which connected with the surrounding cells. The microfilament increased, elongated, and changed from reticulodromous to sarciniform, which reached to the pseudopods. The nucleus were different in size .(2) As shown by the inverted microscope and the cell growth curve, comparing with the controlgroup, cells of each test group increased evidently. The cellular proportion of each test group increased in S phase and G2 ~M phase, and decreased in Go~Gi phase significantly, but there was no considerable interations between LN and EGF;(3) As shown by the morphological observations, the cultured cat corneal endothelial cells formed an integrated membrane, and attached to the Descemets membrane closely, which was similar to the natural tissue. The cells connected tightly to each other, and some of them arranged in hexagon approximately.

结果：(1)层粘连蛋白组处于G_2～M期细胞比例较对照组显著提高，Go～G_1期细胞比例显著下降，提示层粘连蛋白促进内皮细胞DNA合成，及细胞分裂增殖；光镜下，对照组细胞分布成团状，细胞密度较低，细胞间连接紧密，细胞内微丝结成网状，细胞核大小一致；与对照组相比，层粘连蛋白组细胞生长旺盛，细胞密度高，向周边伸出大量板状及丝状伪足，细胞内微丝增多、拉长、集结成束，伸入伪足中，细胞核形状大小不一致；(2)倒置显微镜观察及细胞生长曲线显示，各组细胞数目随时间增加而明显增多，各实验组较对照组增生显著，EGF和LN联合应用组各时间点细胞数目最高；实验组处于S期和G_2～M期细胞数目增加，Go～G_1期细胞数目减少；提示EGF、LN单独及联合应用均可促进细胞增殖，但尚不能认为二者有交互作用；(3)倒置显微镜下，组织培养的猫角膜内皮细胞排列成密集的单层，细胞间连接紧密；组织学观察发现，培养的猫角膜内皮细胞形成完整的内皮层，贴附于脱水基质的后弹力膜上，与正常的角膜内皮组织结构相似；扫描电镜下，组织培养的猫角膜内皮细胞间紧密镶嵌排列，可见某些细胞呈近似六边形排列，细胞大小不甚一致，胞核清晰。

This paper summarizes pluton growing pattern and formation process into central, biacentrol, lateral, irregular and multi-central growth. The volume accretion may be explicated by the growing curves.

岩体的生长方式、形成过程可概括为中心式、偏心式、侧向式、不规则式、中心多点式，生长量特点可以用生长曲线表述。

Method］mscs(5×106) were cultured combining with gdabm in vitro in centrifuge tube, tgf β was added to collagen and attached to gdabm. culture tube was centrifuged in 600 r/min, 10 times/d, 10min per time. the morphological characters, cell proliferation were detected.

方法］将 mscs与复合转化生长因子-β的胶原共同混合后培养于三维软骨支架材料上，离心管内培养，10次／d，以600 r／min离心10 min.8 h、24 h、72 h、 4 d、7 d进行倒置显微镜形态学观察、扫描电镜观察。1～8 d采用mtt法检测细胞增殖活性，描绘生长曲线。

Beijing Fatty Chicken, Langshan Chicken and Small-tailed Han Sheep were selected as experimental material. Fibroblast library was constructed through tissue confluency culture and cell freeze technology. Growth dynamics, genetic stability and contamination of of cross breeds etc.were detected through growth curve, chromosome analysis, isoenzyme analysis etc. Cloning and sequence of gene GPAT of Beijing Fatty Chicken was analyzed by cloning technology and software related.

本论文以北京油鸡、狼山鸡、小尾寒羊为研究对象，采用组织块贴壁培养法和细胞冷冻技术构建成纤维细胞库，采用生长曲线、染色体分析、同工酶分析等方法对细胞生长动态、遗传稳定性、种间交叉污染等进行检测；采用基因克隆技术和相关分析软件对北京油鸡GPAT基因进行克隆和序列分析。

METHODS The inhibitory effect of nobiletin on proliferation of SMMC-7721 cells was assessed by MTT analysis and growth curve assay. Morphological changes under microscope were observed by Giemsa staining. Hepatic cancer H22 model in mice was performed through subcutaneous inoculation of Right-Sidedness Axilla of KM mice. Different dosages of nobiletin 125, 250, 500mgkg^(-1 were injected by intragastric gavage everyday.

不同浓度的川陈皮素作用于人肝癌细胞SMMC-7721细胞，用MTT法、细胞生长曲线实验研究其对SMMC-7721细胞的生长抑制作用，Giemsa染色观察细胞形态变化，初步研究其体外抑瘤作用；建立小鼠H22肝癌移植性实体瘤模型，研究川陈皮素对肝癌的体内抑制作用。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。