用间接免疫荧光染色结合流式细胞技术检测细胞表面DR4和DR5分子表达;
The expression of cell surface-bound DR4 and DR5 were determined by indirect fluorescence staining and flow cytometry analysis.
采用双标记流式细胞分析技术,分别检测各组小鼠脾脏及肠系膜淋巴结(MLN)CD80M和CD86 M的表达。
The number of CD80/CD86 M of spleen and mesenteric lymph node(MLN) were determined by double-label FCM method.
并用TUNEL技术和流式细胞仪检测了相关淋巴细胞的凋亡。
TUNEL and flow cytometry were used to detect apoptotic cells.
方法用流式细胞仪检测缺血缺氧后不同时间点星形胶质细胞细胞周期变化,并用荧光免疫细胞化学技术测定胶质细胞纤维酸性蛋白(GFAP)和增殖细胞核抗原(PCNA )的表达水平。
Methods We measured the astrocyte cell cycles in different time after ischemia and anoxia by flow cytometry and detected the levels of GFAP and PCNA with fluorescence immunocytochemistry.
方法用流式细胞仪检测缺血缺氧后不同时间点星形胶质细胞细胞周期变化,并用荧光免疫细胞化学技术测定胶质细胞纤维酸性蛋白(GFAP)和增殖细胞核抗原(PCNA )的表达水平。
Methods We measured the astrocyte cell cycles in different time after ischemia and anoxia by flow cytometry and detected the levels of GFAP and PCNA with fluorescence immunocytochemistry.
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