方法：采用配制不同条件海水加富培养液培养裸甲藻，计算藻细胞密度来考察裸甲藻的生长情况。
Methods: Gymnodinium was cultivated in rich sea water and the growing conditions were studied by cells density.
结论用明胶包被培养皿，在培养液中加入肝素、内皮细胞生长因子及高浓度的胎牛血清可获得较纯的内皮细胞。
Conclusion the suitable condition for endothelial cell were use of gelatin coat culture dishes, and adding of heparin, endothelial growth factor and highly fetal serum into culture media.
结论T1A ，T2A条件培养液对PC12细胞有刺激生长作用，说明T1A ，T2A对中枢神经再生有积极作用。
Conclusion T1A or T2A conditioned medium can promote PC12 cells'growth, suggesting that T1A and T2A are helpful to neural regeneration.
用不含血清和含0.5%血清的培养液直接饥饿指数生长期的成纤维细胞，细胞数量先是略有增长，然后逐渐下降。
After used medium in eluding 0.5% NCS and without NCS direct starvation, the Numbers of fibroblast first in creased slightly, then gradually decreased.
培养液覆盖培养层，培养液包括至少一细胞成长因子，以促进一细胞沿所述的碳纳米管生长。
The culture solution covers the culture layer and comprises at least one cell growth factor which promotes cells to grow along the carbon nanotubes.
培养液覆盖培养层，培养液包括至少一细胞成长因子，以促进一细胞沿所述的碳纳米管生长。
The culture solution covers the culture layer and comprises at least one cell growth factor which promotes cells to grow along the carbon nanotubes.
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