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。
Methods Wright's staining coated pieces with puncturing marrow of 98 cases were tested by oil lens of OLYMPUS microscope made in Japan.
方法瑞特染色用日本产的显微镜对98例患者的骨髓穿刺涂片进行油镜检查。
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 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 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。
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 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 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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