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02:05 min
July 26th, 2024
DOI :
10.3791/202314-v
* These authors contributed equally
Transcript
首先,取在 T25 培养瓶中生长的神经元进行共培养。用 5 毫升含有胰蛋白酶和 Dnase I. 的 versene 溶液替换培养基,加入 0.5 毫升胎牛血清以中和胰蛋白酶和 Dnase I.将细胞转移到 15 毫升锥形管中。用 5 毫升完全 neurobasal 培养基洗涤培养瓶一次,以最大限度地增加收集的神经元。
然后,在 4 摄氏度下以 300 G 离心细胞悬液 5 分钟。弃去上清液后,将细胞沉淀轻轻重
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