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Methods Toluidine blue was used to stainingMC and fluorescence method to deterˉmin content of histamine.

方法采用甲苯胺蓝方法显示肥大细胞,荧光方法测定组胺含量。

Four rats in each group were re-anesthetized. They were killed and their brain was gained. Survival neurons were detected with toluidine blue staining.

然后每组取4只大鼠,采用相应的麻醉剂进行麻醉后处死取脑,甲苯胺蓝染色检测半暗带内的存活神经元。

The staining of safarnin O and toluidine blue was made weaker in both groups at 4 day and 4 week postinjuriously.

模型组和对照组番红"O"和甲苯胺蓝染色均逐渐减弱,但在相同时间,对照组染色相对淡。

RESULTS: The levels of toxicity ranged from 0 to 1 grade. HE staining and toluidine blue staining demonstrated that PDLCs could adhere and proliferate on the surface of SIS in good condition.

结果:MTT法检测证实细胞毒性为0~1级,材料无细胞毒性;HE染色和甲苯胺蓝染色可见PDLCs在SIS表面和内部均生长良好,显示SIS具备良好的生物相容性。

Toluidine blue stain, the BVF by computer image analysis was similar to Micro-CT.

苯胺兰染色后,经过图像分析所得的骨痂体积比与Micro-CT检测所的结果接近。

Toluidine blue staining and typeⅡcollagen immunohistochemistry staining also showed positive results in both groups, but they were more significant in the experimental group.

石蜡切片HE染色可见类似正常软骨的组织学特征,甲苯胺蓝染色及Ⅱ型胶原免疫组化染色阳性,实验组的阳性染色程度较高。

Collagen Ⅱ immunohistochemistry and toluidine blue staining had a weak expression on primary and subcultured cells.

原代和传代后细胞Ⅱ型胶原免疫组织化学和甲苯胺蓝异染反应均较弱。

The other cartilage specimens were stained with hematoxylin and eorin、toluidine blue to examine the histological structure under light microscopy.

另3 只动物的软骨标本分别行HE 染色和甲苯胺蓝染色,光镜下观察修复软骨的组织学结构。

Carbon nanotube ; toluidine blue ; synergistic effect ; glucose oxidase

碳纳米管;甲苯胺蓝;协同作用;葡萄糖氧化酶

Secondly, the author prepared polypyrrole using emulsion polymerization method as well as water soluble polyaniline by adding a small amount of surfactant. Both knids of materials are used as sensing film of QCM trimethylamine gas sensors, respectively.

其次,采用乳聚法和添加少量表面活性剂诱导的方法分别制备了聚吡咯、水溶性聚苯胺,并将它们作为敏感膜材料制作了QCM气敏传感器。

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