The characteristics of treated cells were assayed by immunocytochemistry staining analysis.
用免疫细胞化学方法分析诱导前后的细胞表型特点。
Neuronal specific proteins in treated cells were assayed by immunocytochemical staining analysis.
免疫细胞化学检测诱导后的细胞中神经细胞特异蛋白。
After systematically study on the main factors involved, an AFLP silver-staining analysis system suitable for walnut genomic DNA was established.
通过对内切酶用量、酶切时间、连接时间、稀释倍数等的研究，建立了适于核桃分析的AFLP银染技术体系。
The methods of analysis of the chromosome aberrations mainly include routine staining method, G-banding method and FISH technique.
目前染色体畸变分析方法主要包括常规染色法、G显带法和FISH技术等。
Conclusion PKH26 staining combined with fluorescent antibody labeling and flow cytometry were powerful tools for analysis of proliferation of lymphocytes and their subsets.
结论PKH26染色结合荧光抗体标记和流式细胞术，是分析淋巴细胞及其亚群增殖动力的有力工具。
Methods: VEGF-C protein expression in benign and malignant oral lesions was investigated with an immunohistochemical staining assay, followed by light microscopic examination and image analysis.
方法：采用免疫组化染色，光镜及图像分析观察并确定VEGF - C在正常口腔粘膜、白斑及鳞癌等组织中的表达。
Cardi ac histological analysis was performed by staining with hematoxylin.
苏木精染色进行心脏组织学分析。
The area of atherosclerotic plaque was measured by image analysis after oil red o staining.
用油红o染色法和图像分析法测量小鼠动脉粥样硬化斑块面积。
Methods:The techniques including G banding, karyological analysis, PCR amplification and silver staining were used.
方法：应用染色体G分带、核型分析和PCR及银染技术。
The neurite outgrowth of motor neurons was detected by NF-200 immunohistochemical staining and computer image analysis system to measure the lengths of nervous process.
采用NF- 200免疫组织化学染色并进行图像分析，测定神经突起主干长度。
Subsequently we identified the expanding cells by alkaline phosphatase staining, karyotype analysis and the formation of embryoid body which are typical characteristics of ESCs.
采用碱性磷酸酶染色、核型分析、类胚体实验对扩增细胞进行ESC鉴定。
Statistical analysis was performed to determine the relationship between staining of denture and the above...
采用统计学方法，分析全口义齿着色与上述因素的关系。
Methods Three-colour direct immunofluorescence staining and multiparameter flow cytometry were used for analysis of 13 samples of immunophenotyping of multiple myeloma patients.
方法采用三色免疫荧光直接标记法及多参数流式细胞术分析13例多发性骨髓瘤的免疫表型。
The specificity of the purified polyclonal antibody was identified by indirect fluorescence staining and FCM analysis.
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。
Pathological staining and image analysis were used to determine the perimeter and the area of left ventricular cavity, and myocardial nuclei number and collagen content per unit area;
病理染色图象分析测定左室腔周长和面积、单位面积内心肌细胞核数、单位面积内胶原的含量；
Methods Immunohistochemical staining combined with the micro-image analysis and immunofluorescence histochemical double-staining technique were used.
方法免疫组织化学染色结合显微图像定量分析和免疫荧光双重染色。
Further, he staining and immunofluorescence technique were used for morphometric analysis of islets in normal and HD mice.
并应用HE染色和免疫荧光技术分析正常和HD小鼠胰岛形态学差异。
Purity analysis after immunofluorescence staining revealed that the ratio of number of A2B5-positive cells to that of DAPI-positive cells was 98.14%.
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%。
Methods HE staining and immunohistochemical staining technology (S-P method) were used to do retrospective analysis for 52 cases of fibrous dysplasia, which had morphologic abnormalities.
方法用HE及SP法免疫组织化学染色对5 2例形态学变异的纤维结构不良作回顾性分析。
Methods immunohistochemistry in 52 cases of nasopharyngeal carcinoma PTEN gene expression, the use of PCR SSCP silver staining, DNA sequencing analysis to detect PTEN gene mutation in exon 5, 8.
方法采用免疫组化检测52例鼻咽癌中pten基因的表达，利用PCRSSCP银染、DNA测序分析等方法检测pten基因第5、8外显子突变。
The expression of cell surface-bound DR4 and DR5 were determined by indirect fluorescence staining and flow cytometry analysis.
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 confocal laser scanning microscopic analysis showed the double staining for EAAT1 and GFAP.
共聚焦扫描显微镜下可见EAAT1与GFAP双标记的星形胶质细胞。
Method: Slices of surgically resected human mandibular bone containing healthy teeth received fibers special staining, and then were measured by image analysis methods.
方法：选取外科切除含健康牙的人下颌骨块，进行纤维特殊染色，用体视框和图象分析法测量。
Methods Nude mice were performed partial hepatectomy model, the MVD and VEGF was detected by using immunohistochemical staining and image analysis.
方法采用切除裸鼠肝左叶和中叶观察肝肿瘤生长情况，以免疫组化和图像分析检测肝癌组织MVD、VEGF的表达。
Hepatic COX? 2 expression were measured with immunohistochemical staining and image analysis in all groups. Levels of serum ALT were determined.
免疫组化图像分析法测定各组肝组织COX ？2的表达，同时测定血清中谷丙转氨酶(ALT)水平。
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。
Immunohistochemical staining and image analysis were used to detect the number of the positive neurons and the mean optical density and the percentages of SP positive cells in the DRG.
免疫组织化学方法结合图像分析检测各组脊神经节sp的阳性神经元数和平均光密度，并计算阳性细胞百分率。
Hepatic COX2 expression were measured with immunohistochemical staining and image analysis in all groups. Levels of serum ALT were determined.
免疫组化图像分析法测定各组肝组织COX2的表达，同时测定血清中谷丙转氨酶(ALT)水平。
The scaffolds were investigated by histological staining, SEM observation and porosity measurement, water absorption rate analysis. MTT test was also done to assess cytotoxicity of the scaffolds.
冷冻冻干后，对支架材料进行组织学及扫描电镜观察，测定支架孔径和孔隙率、吸水率，并采用MTT法分析支架浸提液毒性。
The scaffolds were investigated by histological staining, SEM observation and porosity measurement, water absorption rate analysis. MTT test was also done to assess cytotoxicity of the scaffolds.
冷冻冻干后，对支架材料进行组织学及扫描电镜观察，测定支架孔径和孔隙率、吸水率，并采用MTT法分析支架浸提液毒性。
应用推荐