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寻求外泌体透射电镜固定方法?

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发表于 2016-10-14 10:34:57 | 显示全部楼层

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The samples were dissolved in HEPES (4-[2-hydroxyethyl]-1-piperazine ethanesulfonic acid) buffer, and a drop of the suspension was placed on a sheet of parafilm(一张保鲜膜). A carbon-coated copper grid(碳涂层铜网格) was floated on the drop for 10 seconds. Then, the grid was removed, and excess liquid was drained by touching the edge of the grid against a piece of clean filter paper. The grid was touched onto a drop of 2% uranyl acetate(醋酸双氧铀)or phosphotungstic acid(磷钨酸), pH 7.0, for approximately 5 seconds, and excess liquid was drained off. The grid was allowed to dry for several minutes and then examined using a JEM-1200 EX microscope (JEOL, Akishima, Japan) at 80 kiloelectron volts.
我还没有做出很好看的电镜,因为样品提取的不好,杂质比较多,我们可以相互交流
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发表于 2016-10-18 16:36:56 | 显示全部楼层
陆峰彬 发表于 2016-10-16 11:37
你这个方法好像没有用到固定。请问你那个保鲜膜是细胞房那种防污染的透明膜?还有你用的铜网是普通铜网? ...

我们这边做电镜都没有固定,大部分文献里也没有用到固定,铜网做电镜的老师会给
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