Oil red staining and alizarin red staining both demonstrated positive reactions but not in control groups.
成骨诱导后茜素红染色阳性，对照组为阴性。
The results of oil red staining indicated that a small quantity of lipid droplets in sebocytes, and immunohistochemistry staining of CK4.62, EMA were positive in subculture sebocytes.
油红染色显示，皮脂腺细胞含有少量脂质小滴，CK4.62、EMA免疫组织化学染色均为阳性；
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；
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。
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 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。
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。
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。
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 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。
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