盖玻片

作者在制作阴道毛滴虫染色标本中，采用盖玻片推片，在染液的配制、比例、浓度、pH值上作了适当的调整，使虫体各部位着色清晰。

By changing / improving the preparation , ratio , concentration and pH value of the staining solution , the cultured specimen of Trichomonas vaginalis was better observed .

将软骨细胞分别接种于PGA无纺网支架和盖玻片上，待细胞充分贴壁后，支架和盖玻片均被随机分为两组，实验组在循环压力下培养，对照组在普通条件下培养。

After adherence , the scaffolds and cover slips were both divided into 2 groups .

在这部分实验中，我们自己制作了微流控芯片，芯片通道采用PDMS膜制成，然后将膜封接到盖玻片上。

In this part , the microfluidic chip was made of PDMS . The PDMS channel was fixed on the cover glass .

结果生长在包被LN的盖玻片上48小时的SEC，其窗孔数目及大小均比生长在型胶原上的SEC明显降低（P<0.05）；

Results The average number of fenestrae and their diameter in the SECs cultured on laminin coated coverslips were significantly lower than those on collagen type ⅰ coated coverslips .

显微镜电感耦合器件CCD前面安装一个透射光栅，我们还成功地追踪到了脱水琼脂糖修饰的表面与盖玻片之间溶液中的单个动态量子点的光谱。

We successfully tracked the spectral images of single dynamic QDs in the aqueous solution between the dried agarose-modified surface and the cover slide by the standard epi-fluorescence microscopy with a transmission grating installed in front of the charge-coupled device .

方法用胶原酶原位灌注、Percoll不连续密度梯度离心法分离大鼠的SEC，并加入包被有型胶原或层粘连蛋白（laminin，LN）基质的盖玻片上培养。

Methods By in situ collagenase perfusion and two step percoll gradient centrifugation , SECs were isolated from normal Wistar rats and cultured on collagen type ⅰ or laminin coated coverslips .

方法采用联合法将虫龄为24d的日本血吸虫成虫细胞接种于小盖玻片上，培养于常规培养基中。

Methods The cells from S. japonicum were inoculated on the small glass cover slips .

4个组都在37℃恒温培养箱里培养60分钟，取出盖玻片进行PAS反应并显示SDH活性。

Control group . The four groups were cultivated for sixty minutes at 37 ℃ in a thermostat . Then PAS reactions were operated and the activity of SDH were tested on cover glasses .

将数个鸡胚背根节按一定间隔种植在内置生长基质盖玻片的35mm培养皿中，加人适量培养液，置于CO2。

Several DRGs were seeded at certain intervals into a 35 mm culture dish in which growth substratum coverslip has been placed and suitable volume of culture mediums was added into the culture dish .

在常规培养瓶中附贴小块盖玻片，使CNE细胞株在玻片上生长。培养6、24小时和2、3、4天后，各取出附在玻片的瘤细胞进行扫描电镜观察。

CNE cells were cultured on cover glasses placed in the culture flasks , and were examined under scanning electron microscope 6,24 , 48,72 , and 96 hours after cultivation .

他用盖玻片来准备永久标本。

He uses cover slips to prepare permanent visual records .

长有细胞的盖玻片处理后进行细胞免疫荧光染色。

Cells on cover slips were subjected to immunofluorescence staining .

支气管肺泡灌洗液细胞定量&显微镜盖玻片法与细胞离心制片法之比较

Quantification of Cells Recovered by Bronchoalveolar Lavage : comparison of microscopic glass

注意：盖玻片是很容易坏掉的！

Be careful : the cover glass is fragile !

用盖玻片培养法表明，该组份有促进神经元突起生长的作用。

Using coverslip culture method , above M CM also showsneurite promoting effects on the neurons .

利用盖玻片对生物膜的显微观察表明生物膜含有多糖成分。

The microscopic analysis of biofilms formed on glass coverslips revealed that the biofilm contains polysaccharides exopolysaccharides .

并利用扫描电镜观察比较处理组与对照组间盖玻片上大肠杆菌生物膜形态上的差异。

The different changes in the biofilm were compared between the treated groups and the control group with scanning electron microscope .

取指数生长期细胞，胰酶消化计数活细胞数，按一定数量滴加单细胞悬液于盖玻片上，盖上培养皿上盖。

Exponentially growing cells were trypsinized , counted for the live ones and planted onto the cover glasses in definite cell number .

取包被组二次传代后的神经球滴在包被有多聚赖氨酸的盖玻片上观察神经干细胞生长情况。

Neurospheres of coated group after the2nd passage were cultured in polylysine-coated slides so as to observe the growth characteristics of NSCs .

方法：取受检者睫毛每人5根，置洁净载玻片上，滴一滴甘油，盖上盖玻片镜检。

Methods Five cilia of each subjects were taken and put on the slide with glycerin , which were test ed by microscopy .

冰冻切片法在割断豚鼠腮腺血管铸型中的应用一种在盖玻片上进行组织切片原位杂交的方法

Application of Frozen Section Technique to Study the Vascular Casts of Guinea Pig Parotid Gland In Situ Hybridization of Tissue Sections on Cover-slips

传2代后，胰酶消化，置于6孔板内，每孔细胞数量5×105,2d后细胞贴壁生长于盖玻片上，分别转染Ad。

After 2 passages , the cells were put into a 6-well plate after digested with pankrin , with 5 × 105 cells each well .

3以盖玻片接种细胞作为阴性对照，在不同烤瓷合金表面分别接种人牙龈成纤维细胞。

HGFs were seeded onto the surface of various types of ceramic alloys as well as onto the cover slips , which served as negative control .

结果①调查显示我省县级以上医院有74.8%仍用普通玻片（或加盖玻片）直接镜检进行尿液沉渣分析检查，只有25.2%的医院采用商品化尿液沉渣检测系统。

All laboratories were asked to test them and give the feedback . Results The survey clearly demonstrate 74.8 % of district hospitals still use the glass slide ( or with coverslip ) with microscope to do urinary sediment test . The rest of 25.2 % groups use commercial systems .