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- 与 staining 相关的网络例句 [注:此内容来源于网络,仅供参考]
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There were infiltration of inflammatory cells inside nerve tissue and perivascular cuffings in HE staining. In trichrome staining, the axon with inhomogeneous chromatosis was swollen and beaded-discontinued; The myelin was porous and partly disaggregated.
HE染色发现神经组织内炎细胞浸润,血管&袖套&样病灶形成;三色染色可见轴突肿胀,呈串珠状,且不连续,着色不均匀;髓鞘结构层次紊乱,疏松,崩解。
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In situ terminal transferase-mediated dUTP nick end-labeling was used to detect the apoptosis of SMC in these two groups; We compared the elastic fibers, collagenic fibers, reticular fibers by special staining in the two groups by special staining.
结果 (1)常规HE染色组织学观察颅内囊性动脉瘤瘤壁均已丧失正常脑动脉壁的三层结构,表现的基本组织病理变化为损伤、变性、修复同时存在。
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The uranine staining can be used to observe the whole growing phases of Sphaerotheca fuliginea, while aniline blue staining is suitable for conidial observation.
荧光素钠可以观察到菌体整个发育阶段。苯胺蓝只适合于前期菌体入侵过程的观察。?
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ERK1/2 immunohistochemistry positive staining coloration in cornu dorsale medullae spinalis of rats was Buffy color.Positive cells distributed in gray nucleus that nerve cell concentrated,and deep staining region localized at the nucelus of neurocyte.
针刺前后脊髓未见明显形态学改变。2、光镜下观察,大鼠脊髓背角ERK1/2免疫组化反应显色呈棕黄色,阳性细胞分布于脊髓灰质神经元集中的部位,针刺后深染部位向胞核集中。
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The aim of this study was to clarify the role of pathologic predictors by using immunohistochemical staining and Elastica van Gieson staining.
本研究的目的就是要阐明免疫组化和EVG弹力纤维染色评价这些病理学参数的作用。
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Methods The chronic ocular hypertention rat model was made by cauterizating three episcleral veins.Rats were divided into control group,high level PROG group,middle level PROG group,low level PROG group according to different concentrations of PROG injected intraperitoneally.The left eye was model eye and the right eye was control eye.Three months later,the animals were executed and the eyeballs were enucleated.The RGCs were detected by HE staining and Thy-1.1 immunohistological staining.
通过烧灼3条巩膜上静脉制作慢性高眼压动物模型,此模型按腹腔注射不同浓度的孕酮而分为高、中、低浓度孕酮注射组及空白对照组,左眼为模型眼,右眼为自身对照眼,3个月后处死动物,取眼球制石蜡切片,行HE染色、Thy-1.1免疫组化染色及TUNEL原位凋亡检测。
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Eamamined by fluorescin staining and Giemsa staining, 0.2 mg/L colcemid was considered suitable for inducing high percentage of micronuclei in A9 (neo12) cells, without causing death of a mass of cells.
通过荧光染色和吉姆萨染色分析,结果表明,A9(neo12)细胞经0.2 mg/L秋水仙素酰胺处理48 h后,89﹪的细胞产生微核化,每个细胞平均形成10个微核。
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After treatment,the various stained indexes such as liver hematoxylin and eosin staining,SDHase and ATPase histochemic staining,and the conten...
调节三羧酸循环,促进脂肪酸的β氧化和肝内甘油三酯的转运是肝脂消方抗肝脂肪变性的重要作用机制。
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Results Microscopically, different degrees of hepatocytic degenerative changes and hyperplasic fibrous tissue and typical false lobule formation could be seen. Timm's staining result showed uneven distributed black granular deposits in the hepatocytes. No specific PAS staining was observed. Utrastructurally, the mitochondria were increased in volume and dramatically different in shape. The number of lysomes were increased.
结果 光镜下肝细胞表现为不同程度的退行性变,胶原纤维增生以及典型假小叶形成;Timm's染色阳性,发现不均匀分布黑色颗粒或团块样物质沉积;PAS染色则普遍缺乏特异性染色;超微结构显示线粒体形态多样,体积增大,溶酶体增多,粗面内质网管腔扩张,附着核糖体的脱颗粒,以及胞质水肿,质膜溶解。
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Methods:Animal models of 25 adult mixed breed dogs were established by transverse osteotomy at bilateral iliopectineal crest,which were fixed with ATMFS anterior column connector and steel plate respectively. The animals were examined at 2,4,6,8,and 12 weeks by X-ray,macropathological observation and biomechanical test. Tetracin fluorescent labeling,HE staining,Masson triad colour staining,in situ hybridization and immunohistochemical method were performed and histological image analysis were applied.
建立犬双侧骨盆弓状线骨折的动物模型,分别采用ATMFS前柱固定器和5孔重建钢板内固定,于术后2、4、6、8、12周分别行影像学检查、大体观察及生物力学测试;采用四环素荧光标记法、HE染色、Masson三色染色法、原位杂交法、免疫组织化学法进行组织学观察并图像分析;采用RT-PCR法检测骨折端不同时期骨钙蛋白和核心转录因子mRNA相对表达量的变化。
- 推荐网络例句
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This one mode pays close attention to network credence foundation of the businessman very much.
这一模式非常关注商人的网络信用基础。
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Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.
扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。
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There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.
双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。