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- Methods Primary culture of cortical neurons was made from newborn rats.Immunocytochemical and electronic micoscopic methods were used to identify the cultured neurons. 方法体外原代培养新生大鼠大脑皮质神经元,应用免疫细胞化学法及电子显微镜鉴定神经元。
- primary culture neuron 原代培养神经元
- primary cultured neuron 原代培养神经元
- It was a key for HPLF primary culture using plastic bottle, FBS and RPMI1640. 商品塑料培养瓶、胎牛血清、RPMI1640是提高体外HPLF培养成功率的关键。
- To study the effects of hyperthermia on the neuroepithelium in primary culture. 目的：研究高温对神经细胞生长发育、存活、凋亡的影响。
- A primary culture of myoblasts may be prepared by excising skeletal muscle tissue from 10to 30 day old rat embryos. 制备成肌细胞的初级培养物，可以将10-30天的大鼠胚胎骨骼肌组织剪切下来。
- A primary culture of myoblasts may be prepared by excising skeletal muscle tissue from 10 to 30 day old rat embryos. 制备成肌细胞的初级培养物,可以将10-30天的大鼠胚胎骨骼肌组织剪切下来。
- Objective: To establish an easier and better primary culture technique suitable to neurons of newborn rat cortical tis-sure. 摘要目的：建立一种简单、较理想的新生大鼠皮层神经元体外原代培养方法。
- Objective To establish a method for the primary culture of bovine retinal capillary pericytes. 摘要目的：建立牛视网膜毛细血管周细胞原代培养的方法。
- This technique for the primary culture of cortical neurons is an ideal good technique for the general labs. 本方法适合普通实验室进行大鼠皮层神经元体外培养。
- Tsuji T,Karasek M.A procedure for the isolation of primary culture of melanocyte from newborn and adult human skin. 赵辨;黄秋玲;毕志刚;等.;人正常黑素细胞体外纯培养及其生物学鉴定
- Conclusions: Hyperthermia may induce apoptosis of neuroepithelium in primary culture. 结论：高温可诱发原代培养神经细胞凋亡。
- Conclusions: It was a key for HDPC primary culture using plastic bottle, DMEM in high glucose and CFBS. 结论： 商品塑料培养瓶、标准胎牛血清、高糖DMEM是提高体外HDPC培养成功率的关键。
- Conclusion It was a key for HPLF primary culture using plastic bottle, FBS and RPMI1640. 结论商品塑料培养瓶、胎牛血清、RPMI1640是提高体外HPLF培养成功率的关键。
- Objective To create a simple and effective primary culture methods for mouse vascular smooth muscle cells(VSMC). 目的建立一种简单方便但高效的血管平滑肌细胞原代培养方法。
- Conclusions The method for the primary culture of hippocampal neurons is a good method for t... 结论本方法适合一般实验室开展海马神经细胞培养。
- Objective:To explore an efficient procedure for primary culture of human oral mucosal epithelial cells. 目的:分析影响口腔粘膜上皮细胞原代培养影响因素,探讨理想的培养条件。
- Methods The primary culture implant of human umbilical arterial smooth muscle cells was adopted. 方法选取人脐动脉原代平滑肌细胞植块培养,得到传代细胞。
- Myoblast cells were primary cultured with method of femur muscle pieces. 取20只小鼠分4组,取股骨肌用肌块法进行成肌细胞原代培养,并重复利用肌块6次。
- Primary cultured neurons 原代培养神经元
