Methods: Primary embryonic rat cortical neurons culture, cytotoxicity assays and biochemistry detection, cell stain for the neuron morphology in microscopy and image analysis.
方法：原代胚胎鼠皮质神经元细胞培养，细胞毒性试验及生化指标测定，细胞染色，显微镜下观察形态学改变及影像分析。
The results of growth hormone (GH) determination, cell stain and computer image analysis showed that cells of both fresh and cryopreserved pituitary were of biological viability.
经生长激素(GH)测定、细胞染色及计算机图像分析，证明胎儿垂体细胞冻存前、后经体外培养均有活性。
A different stain marks nerve cell fibers (bottom), revealing heavy staining in the central region where nerve fiber tracts connect one region of the brain to another.
用一种不同的着色剂标示出了神经细胞纤维(底部)，图中中部着色很重的区域是神经束将大脑的各个不同部位进行连接的部位。
Results Stain for EGFR was detected in all cell types of trophoblasts in GTD and normal chorion villi.
目的研究表皮生长因子受体在妊娠滋养细胞疾病的表达，探讨EGFR对预测葡萄胎恶变的价值。
Methods Normal tissue stain and immunohistochemical stain were used to observe the mast cell and substance P immunoreactivity in dorsal root ganglia.
方法采用常规组织学染色和免疫组织化学染色方法对家兔脊神经节内肥大细胞和P物质免疫阳性反应进行观察。
Methods: 1. Primary rat skeletal muscle satellite cell was cultivated in vitro. The cultured cells were identified with cellular immunochemical stain.
方法：1体外分离培养大鼠骨骼肌卫星细胞，免疫组化鉴定骨骼肌卫星细胞并检测其纯度。
Methods The inhibitory rates of cell growth were tested by trypan blue stain assay in the different conditions.
方法采用台盼蓝拒染法，在不同条件下测定细胞增殖的抑制率。
Methods The cell growth was tested by trypan blue stain assay and the cell cycle was analysed by flow cytometry in the various conditions.
分别采用台盘蓝拒染法及流式细胞术，在不同条件下测定细胞增殖的抑制率及细胞周期的分布。
A cell, especially a white blood cell, having granules that stain readily with basic dyes.
嗜碱白血球一种细胞，特别是一种白色的血液细胞，具有和碱性。
Methods: After establishing a C6/SD glioma model, by using flow cytometric analysis, immunohistochemistry and HE stain three methods, the proliferation kinetics in C6 glioma cell was measured.
方法：建立C6/SD大鼠胶质瘤模型后，应用流式细胞仪检测、免疫组化、HE染色三种方法，研究C6胶质瘤细胞的增殖动力学指标。
We take Trypan blue stain as the index of cell activity and do morphological and functional examination by NBT-reducing and ink- phagocytosing.
台盼蓝染色作为细胞活力指标，用显微镜检，NBT还原实验和墨汁吞噬从形态、功能两方面检测细胞分化情况。
RESULTS : When ferumoxides-TA or MION-46L TA was used, intracytoplasmic particles stained with Prussian blue stain were detected for all cell lines with a labeling efficiency of nearly 100%.
结果：使用ferumoxides-TA或MION-46L-TA标记细胞时，所有细胞的胞浆内均可检测到普鲁士蓝染色颗粒，其标记的效率接近100%。
Methods:The expression of TFAR19 was observed in 17 cases of oral normal mucosa, 60 of oral leukoplakia and 30 of oral squamous cell carcinoma by immunohistochemical stain.
方法采用免疫组织化学方法检测17例正常口腔黏膜、60例口腔白斑，30例口腔鳞癌组织标本中TFAR19蛋白的表达。
There were 3-7 layers cell in epithelium, which were connected with intercellular bridge immunohistochemical stain. They were AE1/AE3 positive;
结果：口腔黏膜具备上皮层和上皮下纤维组织，上皮细胞3～7层，见桥粒连接，AE1/AE3阳性；
Unicellular gland - a goblet cell mucus-secreting. (H &E stain.
单细胞腺--分泌粘液的杯状细胞。
Effect: Activate dermal cell viability, and promote collagen regeneration, speeding up metabolism, decomposition stain.
功效：激活真皮细胞活力，促进胶原蛋白再生，加快新陈代谢，分解色斑。
Effect: Activate dermal cell viability, and promote collagen regeneration, speeding up metabolism, decomposition stain.
功效：激活真皮细胞活力，促进胶原蛋白再生，加快新陈代谢，分解色斑。
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