方法应用流式细胞术和细胞免疫荧光染色技术。
Methods It was studied by flow cytometry and immunofluorescence.
方法：采用细胞免疫荧光染色技术和流式细胞术。
Methods Flow cytometry and immunofluorescence staining technique were used.
长有细胞的盖玻片处理后进行细胞免疫荧光染色。
Cells on cover slips were subjected to immunofluorescence staining.
本文应用HAG封闭小鼠mps吞噬功能，用碳廓清实验和组织免疫荧光染色筛选了增强单核-巨噬细胞系统吞噬功能的药物。
The drugs that can strengthen phagocyte function of MPS was selected by applying hag inhibiting phagocyte function of MPS, using the test of clearance of carbon and immunofluorescence staining.
上述处理后的细胞经间接免疫荧光染色标记后，用激光共聚焦显微镜观察其细胞膜egf受体的聚簇现象。
EGF receptors on the cell membrane were observed under a laser scanning confocal microscope after indirect immunofluorescence staining.
免疫荧光实验结果指出，去除DNA和组蛋白的细胞核和染色体与抗肌动蛋白抗体呈阳性反应。
Indirect immunofluorescence tests showed that the DNA - and histone-depleted nuclei and chromosomes reacted positively with the anti-actin antibody.
间接免疫荧光染色及流式细胞术鉴定多克隆抗体的特异性。
The specificity of the purified polyclonal antibody was identified by indirect fluorescence staining and FCM analysis.
并采用免疫荧光抗体染色技术对5例dmd,2例BMD肌细胞膜上抗肌营养不良蛋白的表达观察分析，以2例正常人的肌组织作为对照。
The patients from 5 DMD and 2 BMD were detected by immunofluorescence technique for analyzing dystrophin located in muscle cell membrane, compared with 2 normal males.
间接免疫荧光染色显示，小鼠早期胚胎细胞对角蛋白抗体呈阳性反应，对波形蛋白和结蛋白抗体呈阴性反应。
Indirect immunofluorescence detection showed that positive reaction of diffuse cytoplasmic fluorescence was seen with antibody to keratin but not with antibodies to vimentin and desmin.
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.
免疫荧光染色检测诱导后的脂肪细胞CD105的表达情况；
The expression of CD105 was detected by immunofluorescent staining.
方法：采用逆转录聚合酶链反应(RT - PCR)、流式细胞仪和免疫荧光细胞染色分析技术分析肺上皮细胞系a549细胞PAR s的表达情况。
METHODS: We used RT-PCR, flow cytometry and immunofluorescence cell staining techniques to observe the expression of PARs on A549 cells.
为了观察肌细胞骨架，对传统考马斯亮蓝染色法进行改良，并与免疫荧光染色法进行了比较。
The paraformaldehyde prefixed-coomassie brilliant blue staining is a convenient cytoskeleton staining method for muscle cell.
免疫荧光染色后细胞纯度分析显示，A2B5染色阳性细胞占DAPI染核细胞的百分比为98.14%。
Purity analysis after immunofluorescence staining revealed that the ratio of number of A2B5-positive cells to that of DAPI-positive cells was 98.14%.
方法：应用流式细胞仪和免疫荧光染色法检测组织因子在纤维肉瘤细胞（HT10 80 ）的表达情况；
METHODS: Expression of tissue factor in tumor cells (HT1080) was analyzed by flow cytometry and immunofluorescence staining.
用免疫荧光和免疫酶染色可以确定感染细胞中沙眼衣原体的包涵体。
The antibodies against TE55 Strain were prepared in mice, which were immunized with purified chlamydia. The antibodies have been used in immunofluorescence and immunoenzymatic staining.
用免疫荧光和免疫酶染色可以确定感染细胞中沙眼衣原体的包涵体。
The antibodies against TE55 Strain were prepared in mice, which were immunized with purified chlamydia. The antibodies have been used in immunofluorescence and immunoenzymatic staining.
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