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培养细胞的超薄切片技术探讨

Journal of Tianjin Medical University(2004)

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Abstract
目的:探讨培养细胞的电镜良好制样和超薄切片方法.方法:乳腺癌细胞系MB-231培养后分成3组:消化离心组、刮除离心组和原位包埋组,比较培养细胞的超微结构特征.结果:原位包埋方法的超薄切片可以清楚地显现细胞为多角形梭形,细胞连接保持良好.其余两组细胞呈圆形、椭圆形,大部分细胞细胞间连接被破坏,分散分布.结论:原位包埋和单层细胞超薄切片方法是电镜下观察培养细胞的最值得推荐的方法.
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Key words
ultrathin sectioning technique,culture cell
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