The cell cycle of MCF-7 was detected by FACS.
用流式细胞仪检测雌二醇对MCF 7细胞周期的影响。
FACS is a quick and sensitive method of identification.
FACS是一种快速而且敏感的鉴定方法。
The chromosome ploidy was analyzed with FACS technique.
使用流式细胞仪(FACS)分析其染色体的倍性。
Apoptosis was analyzed with FACS and fluorescent microscope.
以流式细胞仪和荧光显微镜分析细胞凋亡状况。
The apoptosis of NB4 cell was analyzed by DNA fragments and FACS.
细胞周期分析和DNA电泳研究细胞凋亡。
Some days later, the cells were collected and identified with FACS.
收集培养细胞，以流式细胞仪进行鉴定。
The cell viability was determined by PI staining and FACS analysis.
PI染色法结合流式细胞术检测细胞死亡率。
Human IL-4 biological activity was identified from the culture supernatant by FACS analysis.
经FACS测定证实细胞的培养上清中具有人IL - 4的生物学活性。
Results: Stable expression of AIRE was confirmed by fluorescence microscope, FACS and western blotting analysis.
结果：经荧光显微镜、流式细胞仪及免疫印迹法检测，证实AIRE基因得到了稳定表达。
METHODS The percentage of androgen receptor positive cells were detected by fluorescence activated cell sorter (FACS).
方法应用荧光激活细胞分离器（FACS）检测雄激素受体阳性的细胞。
Method the cytotoxicity of NK was measured by MTT assay and the express of CD antigen on lymphocytes examined by FACS.
方法采用MTT法进行NK细胞的细胞毒试验和用流式细胞仪测定淋巴细胞CD抗原表达。
The cell surface markers(CD31, CD34 and KDR) were detected by FACS analysis at differentiation 4-7 days in cell culture.
第4天到第7天，应用流式细胞仪动态检测粘附细胞表面标志CD34、CD31、KDR。
The gastric mucosa was taken by the experiment. DI and PI was tested by FACS and the period changes of cell was analysed.
留取胃粘膜组织块，流式细胞仪检测DI及PI，并分析细胞周期变化情况。
Furthermore, the effect of proteasome inhibitors and TAP on particle antigens cross presentation was investigated by FACS analysis.
进而，采用流式细胞技术研究了不同蛋白酶体抑制剂以及TAP对噬菌体颗粒抗原交叉呈递的影响。
The FACS analysis revealed that the 21 expressions used a unique combination of muscles that was different from all other expressions.
FACS分析显示，这21种表情涉及到的肌肉运动组合彼此不同，可以作为区分依据。
Cells were characterized by immunohistochemistry, cytochemistry, FACS and ultrastructure to identify and detect the differentiated population and markers.
通过免疫细胞化学、细胞化学、流式细胞分析法及透射电镜对其分化后细胞进行鉴定。
METHODS: Dendritic cells (DCs), induced from peripheral blood mononuclear cells (PBMCs) by cytokines, were confirmed by morphological observation and FACS.
方法：以细胞因子从外周血单个核细胞(PBMC)中诱导树突状细胞(DC)，通过形态学观察和流式细胞术进行鉴定。
Methods: the experimental subjects were divided into GS group, control group and GM-CSF group. FACs technology had been used to determine the apoptosis ratio.
方法：实验分人参皂甙组、对照组和GM -CSF组，采用流式细胞技术测定各组细胞的凋亡率。
FACS analysis demonstrated that about 25% of murine 5 FU prestimulated bone marrow cells could be infected after cocultivation with producing cells in vitro .
经包装获得较高滴度的病毒上清，以共培养的方式感染5-氟尿嘧啶预刺激的小鼠骨髓细胞。
Objective To develop a method for acquisition of efficient and stable retroviral packaging cells on the basis of fluorescence-activated cell sorting (FACS) technique.
目的探讨利用荧光激活细胞分选技术获得有效重组逆转录病毒包装细胞系的方法。
Methods According to the difference of cells s adhesion, a series of method were set up to generate DC and the biological characteristics were studied by he staining and FACS.
方法：根据细胞的黏附性不同，建立了一整套简便的树突状细胞的体外扩增方法，并利用HE染色和FACS研究了其生物学特征。
Four color fluorescence activated cell sorting (FACS) analysis was applied to detect the expression profiles of adhesion molecules and chemokine receptor CXCR 4 on CD34 bright cells.
应用四色荧光活化流式细胞术(FACS)检测CD 34 +细胞其粘附分子及趋化因子受体CXCR -4的表达谱。
Methods ADSC was isolated from fat tissue by liposuction and culture expanded. Cells at passage2 were observed for the expression of HLA, HLA, B7-1, B7-2, CD40 and CD40L by FACs analysis.
方法体外培养人脂肪抽吸术中获取的脂肪干细胞，体外培养至第二代，流式细胞仪检测免疫分子HLA、HLA、B7-1、B7-2、CD40的表达。
Methods According to different adhesiveness of DC in vary period, a simple method was used to generate and purificate DC, and their biology character were identified by Wright staining and FACS.
方法根据不同时期树突状细胞的粘附性质不同，设计简便的树突状细胞的体外扩增和纯化方法，并利用瑞氏染色和流式细胞仪（FACS）鉴定其生物学特征。
Methods According to different adhesiveness of DC in vary period, a simple method was used to generate and purificate DC, and their biology character were identified by Wright staining and FACS.
方法根据不同时期树突状细胞的粘附性质不同，设计简便的树突状细胞的体外扩增和纯化方法，并利用瑞氏染色和流式细胞仪（FACS）鉴定其生物学特征。
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