Adipogenic differentiation of ASCs was assessed by Oil Red o staining.
成脂定向诱导分化后油红“O”染色定性。
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。
The degree of adipogenesis and differentiation were measured by Oil Red O staining extraction assay.
油红O染色提取定量分析细胞内脂肪生成及细胞分化程度；
Oil Red o staining of the ASCs after 2 weeks of culture demonstrated numerous intracellular lipid droplets.
成脂诱导分化2周后，细胞内可见有大量脂滴，油红“0”染色可见胞浆内有大量红染颗粒。
The proliferation and differentiation of preadipocyte were determined by MTT spectrophotometry and Oil Red O staining respectively.
目的探讨苯对胚胎肢芽、中脑细胞分化和增殖的影响及对肢芽器官发育的影响。
The proliferation and differentiation of preadipocytes were determined by MTT spectrophotometry and Oil Red o staining, respectively.
采用形态学观察、mtt比色、油红o染色提取法，比较各组细胞形态以及增殖与分化的效果。
Lipid droplets in cytoplasm were observed by oil red o staining. The contents of intracellular cholesterol ester were detected by enzyme-fluorescence.
运用油红o染色观察细胞浆内脂滴的变化，酶荧光学法检测细胞内胆固醇酯含量的变化。
Results Oil red o stain showed that LCM aggregated in tumor cells and the LCM density of multiple injection group was much higher than that of single injection.
结果油红o染色显示肿瘤细胞内有LCM的聚集，且多次注射L CM组其LCM浓度明显较单次注射组高。
The glucose consumption in 3T3-L1 cells was determined by glucose oxidase(GOD)method. The fat content in 3T3-L1 cells was determined by Oil Red O staining and spectrophotometry.
采用葡萄糖氧化酶法检测3T3-L1葡萄糖的消耗作用，使用油红O染色并通过比色定量分析3T3-L1细胞的脂肪含量。
The osteogenic differentiated cells were positive for alkaline phosphatase (ALP) and the adipogenic differentiated cells displayed accumulation of lipid vacuoles, as detected by oil red o.
定向诱导的成骨细胞表达碱性磷酸酶活性，脂肪细胞内出现明显的脂滴。
The osteogenic differentiated cells were positive for alkaline phosphatase (ALP) and the adipogenic differentiated cells displayed accumulation of lipid vacuoles, as detected by oil red o.
定向诱导的成骨细胞表达碱性磷酸酶活性，脂肪细胞内出现明显的脂滴。
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