培养的细胞可以稳定生长传代。
结论培养的细胞为大鼠肾小球系膜细胞。
Conclusion the cultured cells form the glomeruli of rats were glomerular mesangial cells.
培养的细胞为多边形。
结论：本文培养的细胞为家兔肾脏IMCD细胞。
Conclosion: The primary cultured cell in this study, is IMCD cell of rabbit kidney.
在这种方法中培养的细胞用表皮生长因子刺激不同时间。
For this approach cell cultures were stimulated by EGF for different lengths of time.
在复合支架上培养的细胞能够迁移至支架内部旺盛生长。
The cells seeded on the composite scaffold could migrate to the inside of the composite scaffold and grew well.
迄今为止我们已取得了突变的原代培养的细胞以及蠕虫”。
To date we have made mutant tissue-cultured cells as well as worms.
培养的细胞用70%乙醇固定，流式细胞仪测DNA含量。
The cultured cells were fixed with 70% ethanol, DNA analysis by Flow Cytometry.
培养的细胞具有良好的生物学活性，细胞表型稳定可保持3代；
The chondrocytes cultured in vitro maintained the specific chondrocytes phenotype in the first 3 passages.
硫酸氨基葡萄糖可以抑制这一趋势，促进传代培养的细胞增殖能力。
GS can inhibit the tendency and strengthened the proliferating ability of chondrocytes in serial subcultivation.
实验研究了猪血管内皮细胞体外培养方法并对培养的细胞进行了鉴定。
The present experiment studied the culture methods of swine vascular endothelial cell (SVEC) in vitro.
FAK的磷酸化水平在悬浮培养的细胞中是下降的，这与文献报导一致。
Phosphorylation of FAK was decreased in suspended cells, which is in agreement with previous reports.
结果(1)培养的细胞经形态学观察和波形蛋白sp染色，鉴定为成纤维细胞。
Results (1) the cultured cells identified by morphology and SP staining with vimentin showed the characteristic of fibroblasts.
结果：(1)经形态学、免疫细胞化学鉴定所培养的细胞为大鼠星形胶质细胞。
Results: (1) the characterization of astrocytes was confirmed based on the morphology and positive by the detection of GFAP antigen.
用s 10 0抗体鉴定所培养的细胞并用MTT法检测这些细胞的增殖能力。
Schwann cells were identified by immunohistochemistry with S-100 antibody and their proliferating function was assessed by MTT assay.
进一步研究表明，每次传代时重复使用基质能够使所培养的细胞恢复原来的活力。
Furthermore, it was found that the cultured cells recovered their ability to grow when the substrate was reused every passage.
方法：利用改良消化法对兔晶体上皮细胞进原代培养，对培养的细胞进行形态学观察。
Methods: Using the developed procedure to culture rabbit lens epithelial cells, and the cultured cells were examined morphologically.
实验结果表明，MEM-FA中培养的细胞染色体自发畸变率显著高于完全培养基（MEM）。
The chromosome aberration frequency was increased when lymphocytes were cultured in medium deficient in folate and thymidine (MEM-FA).
该装置可以模拟实际，迅速而准确的对体外培养的细胞作用压力进行检测，且压力值精确可调。
The device can simulate the actual situation and fast and accurately detect the application pressure of cells in vitro culture, with accurate and adjustable pressure value.
结果原代培养的细胞ALP染色阳性区域可以达90%以上，传代培养后细胞阳性率为100%。
Results the area positive for ALP staining is no less than 90% in the primary culture and almost 100% in the subculture.
结论从胚鼠端脑分离培养的细胞具有自我更新能力和多潜能分化能力，为中枢神经系统的干细胞。
Conclusion the cells from fetal rat telencephalon possess multipotency and self renew ability and is believed to be BSCs of the central nervous system.
在培养的细胞中，采用VEGFR - 3和LYVE - 1因子鉴定淋巴管内皮细胞的方法可靠。
It was reliable to use VEGFR-3 and LYVE-1 to identify the lymphatic endothelial cells.
结果：扫描电镜结果表明旋转生物反应器动态培养的细胞生长速度、数量和形态明显优于24孔板静态培养。
Result: the scanning electron microscope result indicated that growth-speed, quantity and modality in the bioreactor were better than that cultured in static 24-pore plate.
最近的试管研究(用培养的细胞组织作研究)，致力于高频辐射是否会妨碍dna修复过程，或对DNA复制过程产生损害。
Recent in vitro studies - that is, studies on cultured cell tissue - have focused on whether radiofrequency radiation might interfere with the DNA repair process and cause damaged DNA to accumulate.
目的：建立体外研究精原干细胞与支持细胞共培养的细胞模型，探讨体外精原干细胞在支持细胞层上的增殖特点。
Objective: to construct cell model of spermatogonial stem cells (SSCs) with Sertoli cell layer in vitro, and study the proliferation characteristic of SSCs in vitro.
此外，骨分化相关特征基因骨桥蛋白OPN在复合支架上培养的细胞中的表达水平也明显高于纯壳聚糖上培养的细胞。
Simultaneously, the osteogenic gene osteopon tin(OPN)of cells cultured on composite scaffolds showed a higher expression level than that on chitosan scaffolds.
目的在本实验室建立小鼠胚胎成纤维细胞培养方法，并在此基础上用培养的细胞检测氯化镉、甲醛等外来化合物的细胞毒性反应。
Objectives: To set up the methods of mouse embryo fibroblasts culture in vitro and to evaluate the toxicity of xenobiotics such as chloride cadmium and formaldehyde by using these methods.
在等渗或高渗负荷下，椎间盘的器官培养模型可以保持器官完整性和细胞活力至少4周。
Organ culture model of intervertebral discs could preserve organ integrity and cell viability at least 4 weeks under iso-osmotic or hyperosmotic loading.
结果表明SRS-82 株的无细胞提取液和其培养上清液的离心沉淀物皆具有致白血病活性。
The results showed that both the cell-free extract and culture supernate from mouse SRS-82 cell line were leukemogenic.
结果表明SRS-82 株的无细胞提取液和其培养上清液的离心沉淀物皆具有致白血病活性。
The results showed that both the cell-free extract and culture supernate from mouse SRS-82 cell line were leukemogenic.
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