The SER of DDP was 1.320 under clone formation assay.
集落形成法结果显示，顺铂辐射增敏比为1.320；
MethodsA clone formation assay was carried out to determine the clonogenicity and regeneration ability of cells.
方法采用有限稀释法，检测细胞单克隆形成的数量及大小；
MTT assay, plate clone formation assay, flow cytometry, and MTS assay were performed to measure the effect of SLP-2 on TE12 cells.
采用MTT比色法、平板克隆形成实验、流式细胞术和MTS比色法分析SLP鄄2对TE12细胞的影响。
Clone formation ability was determined by clony forming assay. Cell cycle and apoptosis were tested by flow cytometry.
通过流式细胞术检测细胞的细胞周期分布和凋亡水平；
Clone formation ability was determined by clony forming assay. Cell cycle and apoptosis were tested by flow cytometry.
通过流式细胞术检测细胞的细胞周期分布和凋亡水平；
应用推荐