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。

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；

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。

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。

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。

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。

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。

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。

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。

Detached primary cells showed alive 100 % staining with 4 % trypan blue .

分离的原代细胞经4% 台 盼 蓝染色后活细胞率为100%；

Methods Cell inhibitory effect were determined by trypan blue dye exclusion test growth curve method and colony formation .

方法应用 锥 虫 蓝排染法、生长曲线测定法、克隆形成实验检测 药物对HL-60细胞生长的影响；

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；

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 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。

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。

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。

Besides trypan blue rejection experiment and MTT method was used to test cytotoxicity and influence on cell proliferation of TAT / 54R / KDEL .

此外，还利用 台 盼 蓝排斥实验和MTT法检测了TAT/54R/KDEL的细胞毒性及其对细胞增殖的影响。

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。

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；

The cell activity was detected with trypan blue staining .

检测细胞活力采用 锥 虫 蓝染色；

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

Manners of cell death were studied with trypan blue staining ;

苔 盼 蓝染色研究细胞死亡方式；

The trypan blue staining showed the alive cells were more than 95 % .

台 盼 蓝染色显示活细胞数>95%；

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。

Methods : Cell proliferation and viability were analyzed firstly by MTT assay and trypan blue exclusion assay .

方法：首先利用MTT法、 台 盼 蓝 拒 染法观察LOV对 HL60、 KG1、 K562细胞增殖及活力的影响。

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。

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。

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。