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。
Method The thermal paper is soaked in the oil red O solution, and the oil red O could colored the fats contained in the fingerprint residue. 方法将检材浸泡在配制好的油红O的显现试剂中,油红可将指纹中遗留的油脂染色从而显现出手印纹线。
The proliferation and differentiation of preadipocyte were determined by MTT spectrophotometry and Oil Red O staining respectively. 通过形态学观察、MTT比色、油红O染色提取法,比较各组细胞形态及增殖与分化的效果。
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 changes of atherosclerosis plaque size were observed by oil red O staining. 油红O染色观察小鼠主动脉根部斑块面积的变化。
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。
Oil red O staining was used to observe the intracellular lipid droplets. 用油红O染色观测细胞内脂质蓄积情况;
Lipid droplets in the cells were stained with Oil Red O. 油红O染色检测细胞内脂滴。
Oil red O became more obvious when concentration was increased. 曲格列酮组随着药物浓度增高,油红O染色明显增强。
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 was used for fat staining. 油红O检测中性脂肪。
Oil Red O Dyeing experiment was used to show the cellular lipid droplets in cells; 油红O染色观察细胞内脂滴的形成情况;高效液相分析法检测细胞内胆固醇含量;
The lipid within endothelial cells was detected with oil red O. 油红O检测细胞内脂质;
The histopathological change in liver ( HE staining, oil red O staining); 肝组织病理变化(HE染色、油红O染色);
Fat droplets in liver tissue stained with Oil Red O were decreased as the doses of CLA increased. CLA组大鼠肝脏切片油红O染色后肝细胞内的红染脂滴随CLA剂量的增加逐渐减少。
This study examined the effect of troglitazone on preadipocyte differentiation by oil red O staining. 油红O染色定量的方法观察曲格列酮对前脂肪细胞分化的影响。
Liver fatty changes were evaluated with oil red O staining. 油红O染色观察肝组织脂肪浸润;
And the cells could be induced to adipocytes, which were positive in Oil red O stains. 成脂诱导后细胞肥大,油红O染色阳性。
By counting cell, determining OD after oil red 0 staining to investigate the effect of CLA on proliferation and differentiation of rat preadipocyte. 利用细胞计数,细胞形态观察和油红O染色OD值测定等方法研究了CLA对大鼠前体脂肪细胞增殖与分化的影响。CLA可减少脂肪细胞数目。
Methods Cell differentiation was determined by Oil Red O staining; 方法油红O染色法测定细胞分化速度;
The lipidoses of aortic sinus was detected by oil red O staining frozen section. 冰冻切片油红O染色检测主动脉窦脂质沉积。
Adipogenic induced for 8 days and oil red O staining was performed. Lipid droplets were found in microscope. 成脂诱导第8天油红O染色,镜下可见被染成橘红色的脂滴。
Oil red O could be specific binding to triglyceride in mature adipocytes. 油红O染料可与脂肪细胞内的脂质特异性结合。
Identification of foam cells: cholesterol content was tested by oil red O staining and oxidase methods, then make conduct qualitative and quantitative analysis of foam cells. 3. 泡沫细胞鉴定,利用油红O染色和氧化酶法细胞内胆固醇含量的测定,进行泡沫细胞定性和定量分析。
The lipid accumulation in kidney was evaluated by Oil Red O staining and quantitative analysis. 油红O染色及酶法检测肾组织内脂质沉积情况。
The cellular lipid accumulation was examined by oil red staining. 2. 油红O染色观察细胞内脂质堆积情况。
The fatty droplets in hepatocytes could be observed by oil red O staining. 采用油红O染色观察处理后肝细胞内脂肪滴变化情况。
Oil red O staining and compared the morphological changes in the structure. 用油红0染色鉴定并比较其形态结构的变化。
The accumulation of lipid droplets in hepatocytes were observed by light microscopy after oil red staining. 当油酸作用肝细胞24h、48h、72h后采用油红O染色观察细胞内的脂滴的积聚情况。