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1)  Combined culture in vitro
体外联合培养
2)  coculture
联合培养
1.
The effect of vascular smooth muscle cells on the adhesion,proliferation and morphology of endothelial progenitor cells in a coculture system;
血管平滑肌细胞对联合培养内皮祖细胞黏附、增殖与形态的影响
2.
In coculture group this immunoreactivity became stronger.
结果显示:各组感觉神经元均产生免疫阳性反应,雪旺氏细胞条件培养基和巨噬细胞条件培养组免疫反应强度与对照组相同,联合培养组免疫反应为强阳性,与巨噬细胞条件培养组相比差别高度显著(P<0。
3.
In this study the influence of shear stress and vascular smooth muscle cells (VSMCs) on the differentiation of EPCs, as well as a role of Akt was detected in a coculture model.
应用EPCs与VSMCs联合培养的平行平板流动腔系统,对EPCs施加5 dynes/cm2切应力,观测切应力和VSMCs对EPCs分化的影响。
3)  co-culture
联合培养
1.
Effect of fibroblasts in co-culture model on smooth muscle cell proliferation and morphology;
联合培养的成纤维细胞对平滑肌细胞增殖和形态的影响
2.
Effect of endothelial cell in co-culture model on smooth muscle cell proliferation and morphology;
联合培养的内皮细胞对平滑肌细胞增殖和形态的影响
3.
Differentiation of Bone Marrow Mesenchymal Stem Cells Co-cultured with Endothelial Cells under Shear Stress
剪切应力下与内皮细胞联合培养的骨髓间充质干细胞的分化
4)  co culture
联合培养
1.
Objective: To investigate the effect of the shear stress on anti coagulation and adhesion ability of ECs co cultured with VSMCs.
目的 :研究切应力对与血管平滑肌细胞联合培养的内皮细胞的抗凝血和粘附的影响。
2.
Objective: To study the anti coagulation function of endothelial cells(ECs) co cultured with vascular smooth muscle cells(VSMCs).
目的 :研究切应力作用下与血管平滑肌细胞联合培养的内皮细胞的抗凝血功能。
3.
Objective: To study the anti stress effect of endothelial cells(ECs) co cultured with vascular smooth muscle cells(VSMCs).
目的 :观察生理切应力作用下与血管平滑肌细胞联合培养的内皮细胞的抗应力能力。
5)  culture in vitro
体外培养
1.
Improvement on culture in vitro of rat cerebral cortical astrocytes;
大鼠大脑皮层星形胶质细胞体外培养方法改良
2.
Progress in research on embryo culture in vitro;
胚胎体外培养的研究进展
3.
Mouse cardiomyocytes culture in vitro;
小鼠心肌细胞的体外培养
6)  in vitro
体外培养
1.
Improvement of cultural method in vitro for Echinococcus multilocularis metacestodes and primary identification of culture product;
泡球蚴体外培养方法的改进及培养产物的初步鉴定
2.
The Modulation of Endochondral Ossification in Rat Nasal Chondrocyte Cultures with 45S5 in vitro;
固骼生对体外培养鼠鼻中隔软骨细胞增殖及骨化的初步研究
3.
Effects of DSPP antisense oligodeoxynucleotide on development and mineralization of mouse molars in vitro;
牙本质涎磷蛋白反义核酸对体外培养牙胚发育、矿化的影响
补充资料:人体外周血淋巴细胞培养

  
  人体外周血淋巴细胞培养
  

  诊法。为 检查患者染色体最简便的细胞培养技术。先于无菌条件下制备RPMI1640 或TC199等常用培养基,加适量小牛血清和PHA(植物血球凝集 素),夏季操作时最好加适量青、链霉素,调pH值为7.0~7.2左右,4℃条件下保存6个月 。检测时,以500IU/ml肝素湿润注射器,抽取患者静脉血1.5~2ml(或取耳垂、指尖或足 跟等处微量血),每份培养基(5ml)内种血0.2~0.3ml,37℃温箱内静置培养72小时,收获 前3~4小时加秋水仙素(或秋水仙胺),最终浓度为0.02μg/ml,使细胞分裂终止于中期。 取出培养物行离心、低渗和固定等一系列细胞学操作获得染色体标本,以Giemsa染色后镜检 ,可作染色体标本的普通分析。现各实验室一般将染色体行G显带或必要的其他多种显带, 以较精确地对染色体标本进行分析。
  
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