The dye Trypan Blue has a remarkable biphasic effect on pinocytosis by yolk sal. 染料锥虫蓝对卵黄囊的胞饮作用具有明显的双向作用。
The well growth and the good biological activities of the retrieved PC12 cells were proved using the MTT and Trypan blue test. 回收微囊化PC12细胞再培养生长良好,MTT法和台盼兰法检测显示细胞具有生物活性。
One of the most successful combinations was trypan blue dye used with a krypton a laser. 实验结果表明,锥虫蓝染料与氪激光器的结合使用是最成功的结合使用之一。
Progress of Trypan Blue Clinical Application in Phacoemulsification 台盼蓝在白内障超声乳化手术中临床应用的研究进展
The cell luminosity factor was detected by flow cytometry, and the cell survival rate was calculated with trypan blue exclusion. 以流式细胞仪测量细胞发光率,以台盼蓝拒染法测算细胞存活率。
The retrieved encapsulated PC12 cells were recultured and their activities were tested by MTT and Trypan blue test. 对移植的微囊化PC12细胞回收后再培养,以MTT和台盼兰检测细胞活性。
Results No cytotoxicity was found in trypan blue staining. 结果锥虫蓝染色未观察到细胞毒性作用。
Methods The inhibitory rates of cell growth were tested by trypan blue stain assay in the different conditions. 方法采用台盼蓝拒染法,在不同条件下测定细胞增殖的抑制率。
Trypan blue staining was used to count the alive cells and to draw a cellular growth curve. 台盼蓝染色计数活细胞数,绘制细胞生长曲线;
There was no significant difference between the results of Trypan blue staining in labeled and unlabeled cells. 标记细胞与未标记细胞的台盼兰染色结果无显著差异。
The cell activity was detected with trypan blue staining. 检测细胞活力采用锥虫蓝染色;
Manners of cell death were studied with trypan blue staining; 苔盼蓝染色研究细胞死亡方式;
Conclusion It is the same effect to detect the activity of the cells between trypan blue and neutral red. 结论锥虫蓝和中性红染色,都能较好地检测细胞的活性。
Results The best staining is by neutral red and trypan blue. 另用80℃水浴3min杀死的阿米巴滋养体作为死亡染色对照。结果中性红和台盼蓝染色效果最好。
Objective To investigate the application of trypan blue in phacoemulsification for the mature cataract. 目的探讨台盼蓝着色前囊膜在成熟白内障超声乳化手术中的应用。
Cell proliferation was mea-sured by MTT assay and trypan blue excluding experiment. 用MTT和台盼蓝细胞排斥实验检测细胞增殖;
METHODS The activity of cultured neurons was measured by MTT assay and trypan blue staining. 方法利用SD大鼠大脑皮质培养神经元,通过MTT法或台盼蓝法测定细胞活力;
Results Trypan blue and indocyanine green adequate-ly stained the anterior capsule in all cases. 结果台盼蓝和吲哚青绿均可充分着染前囊。
Before preservation the thickness of corneas was measured and endothelium was evaluated for morphology and trypan blue staining. 保存前测角膜厚度,做内皮细胞形态学检查和台盼蓝染色。
Staining the separated cells by trypan blue and neutral red. 锥虫蓝和中性红染色检测分离细胞的活性。
Cells were stained by Hoechst 33342 and trypan blue. 采用台盼蓝和Hoechst33342细胞染色液对细胞活力及形态学进行分析。
Trypan blue staining essay showed cell vigor was uninfluenced basically. 台盼兰实验显示细胞的活力基本未受影响。
The growth inhibition of ATO on Bcr-Abl wild type and IM-resistant cell lines were measured by trypan blue exclusion. 本实验采用台盼蓝拒染法观察ATO对Bcr-Abl野生型细胞株和伊马替尼(IM)耐药细胞株的生长抑制作用。
Cardiomyocytes were identified by immunohistochemistry staining of α-actin and we stained cardiomyocytes with trypan blue. 采用α-actin抗体进行免疫组化染色鉴定心肌细胞,用台酚蓝染色检查心肌细胞成活率。