相邻切片进行结晶紫染色显示胶质细胞；
Adjacent sections were stained with crystal violet for demonstration of glial cells.
结晶紫方法测定A值，计算细胞存活量；
ELISA-Crystal violet method was used to detect survival cells.
用结晶紫染色显微镜观察细胞的形态学变化。
Cell morphology was observed under optical microscope with crystal violet staining.
处理细胞后细胞用结晶紫染色并测定od595数值。
Cells were stained with crystal violet at the end of treatment and the OD595 was determined.
存活的细胞固定后用结晶紫染色并测定od595数值。
Surviving cells were fixed and stained with crystal violet and the OD595 was determined.
存活的细胞固定然后用结晶紫并测定OD 595数值。
Surviving cells were fixed and stained with crystal violet and the OD595 was determined.
存活的细胞固定后用结晶紫染色并测定OD595数值。
Surviving cells were then fixed and stained with crystal violet and the OD595 was determined.
存活的细胞固定，结晶紫染色然后读取OD595数值。
Surviving cells were then fixed and stained with crystal violet and the OD595 was determined.
用氧化剂如过氧化氢氧化lcvl，得到结晶紫内酯(CVL)。
The oxidation of LCVL by oxidizing agents such as hydrogen peroxide affords crystal violet lactone (CVL).
研究了非离子表面活性剂对结晶紫-硅钼杂多酸显色反应的影响。
In this paper, the effect of non-ionic surfactant on the decoloration of crystal violet silicomolybdate complex is investigated.
选用高氯酸— 冰醋酸标准液滴定，以电位法或结晶紫指示剂指示终点。
The potentiometric method or the crystal violet indicator was used to indicate the end-point.
选用羧酸类溶剂，采用固相法合成了结晶紫-硼酸系列可逆热致变色材料。
This paper chose some kinds of carboxylic acid as the solvent and a series of crystal violet-boric acid reversible thermochromic paints were prepared by solid phase synthesis method.
细胞增殖抑制试验采用细胞贴壁培养，乙醇固定，结晶紫染色，单层细胞密度计测定细胞密度。
Cell growth inhibition was tested by cell sticking cultivation, ethanol fixation, crystal violet staining and monolayer cell density assaying.
对LDH释放法进行改进，与结晶紫染色法和MTT比色法进行灵敏度、重复性和相关性比较。
LDH release assay was improved and was compared with the crystal violet staining and the MTT colorimetry on sensitivity, repeatability and relateness.
方法：采用结晶紫染色和刚果红染色等方法对几种不同双歧杆菌形成生物膜的能力进行测定和鉴定。
Methods: Biofilm formation ability of several different Bifidobacteriums was determined and identified by crystal violet and Congo red staining methods.
增加微波辐射电压、处理时间和活性炭用量（固液比）均能提高微波—吸附催化法处理结晶紫溶液的脱色率。
The removal rate of crystal violet was directly proportion to the power of microwave, radiation time, amount of activated carbon and initial concentration of crystal violet.
以密胺树脂为壳材、结晶紫内酯-硬脂酸-十四醇组成的热敏变色材料为芯材，采用原位聚合法制备热敏变色微胶囊。
The abamectin microcapsules were prepared by in-situ polymerization process in this work, with melamine-formaldehyde resin and urea-formaldehyde resin as wall materials respectively.
以密胺树脂为壳材、结晶紫内酯-硬脂酸-十四醇组成的热敏变色材料为芯材，采用原位聚合法制备热敏变色微胶囊。
The photochromic microcapsules were prepared by in-situ polymerization, using melamine-formaldehyde resin as wall materials and photochromic materials as core materials.
在吐温- 80存在下，锌与硫氰酸盐、结晶紫生成蓝紫色离子络合物，采用流动注射分光光度法测定海水中的微量锌。
In the presence of Tween-80, trace zinc associates with thiocyanate and crystal violet can form a blue-violet ionic complex, can trace zinc be determined by FIA spectrophotometry.
方法采用核固红结晶紫染色方法，原位末端标记法及形态计量方法定量分析了被动吸烟致金黄地鼠神经管上皮细胞凋亡的变化。
Methods By using the nuclear fast red-crystal violet staining method and situ TUNEL technology, the quantitative changes of apoptosis in neural epithelium in gold hamster were analyzed.
利用结晶紫测定细胞生长的方法，在96孔板培养的小鼠乳腺癌细胞GR2H6中，建立了胰岛素促细胞生长活力的测定体系。
By growing the mouse mammary tumor derived cell line GR2H6 in 96 well plates, we have developed an in vitro bioassay for the growth promoting activities of insulin.
利用结晶紫测定细胞生长的方法，在96孔板培养的小鼠乳腺癌细胞GR2H6中，建立了胰岛素促细胞生长活力的测定体系。
By growing the mouse mammary tumor derived cell line GR2H6 in 96 well plates, we have developed an in vitro bioassay for the growth promoting activities of insulin.
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