• The degree of adipogenesis and differentiation were measured by Oil Red O staining extraction assay.

    O染色提取定量分析细胞内脂肪生成细胞分化程度

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  • 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、o染色提取法,比较各组细胞形态以及增殖分化效果。

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  • Adipogenic differentiation of ASCs was assessed by Oil Red o staining.

    成脂定向诱导分化O染色定性

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  • Methods Wright's staining coated pieces with puncturing marrow of 98 cases were tested by oil lens of OLYMPUS microscope made in Japan.

    方法染色日本产的显微镜98患者的骨髓穿刺涂片进行检查

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  • 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.

    染色显示,皮脂腺细胞含有少量小滴CK4.62EMA免疫组织化学染色阳性

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  • The area of atherosclerotic plaque was measured by image analysis after oil red o staining.

    用油o染色法和图像分析法测量小鼠动脉粥样硬化斑块面积

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  • Oil red staining and alizarin red staining both demonstrated positive reactions but not in control groups.

    成骨诱导后茜素染色阳性对照组阴性

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  • Oil Red o staining of the ASCs after 2 weeks of culture demonstrated numerous intracellular lipid droplets.

    诱导分化2细胞内可见有大量“0”染色可见胞浆内有大量红染颗粒。

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  • 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.

    采用葡萄糖氧化酶检测3T3-L1葡萄糖的消耗作用,使用O染色通过比色定量分析3T3-L1细胞脂肪含量

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  • Lipid droplets in cytoplasm were observed by oil red o staining. The contents of intracellular cholesterol ester were detected by enzyme-fluorescence.

    运用o染色观察细胞变化,酶荧光学法检测细胞胆固醇含量的变化。

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  • The proliferation and differentiation of preadipocyte were determined by MTT spectrophotometry and Oil Red O staining respectively.

    目的探讨胚胎芽、中脑细胞分化增殖的影响及对肢芽器官发育的影响。

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  • The proliferation and differentiation of preadipocyte were determined by MTT spectrophotometry and Oil Red O staining respectively.

    目的探讨胚胎芽、中脑细胞分化增殖的影响及对肢芽器官发育的影响。

    youdao

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