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staining相关的网络例句

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Results Immunohistochemical staining SP methods can help to definitude the histological type and differentiation of astrocytic tumor.

结果:免疫组织化学标记能帮助鉴定组织类型和颅内星形细胞肿瘤的分化程度。

One group was cultured in DEME free of serum; the other in DEME with 10 μg/ml lipopolysaccharides for 6 hours. NF-κB was studied by flow cytometry technique using immunofluorescent staining, and by gel shift assay using γ-32P labeled NF-κB oligonucleotide probe.

取体外培养的第2或3代人角膜基质细胞,同步化后分为2组:无血清的DMEM液培养的不加药组;含质量浓度为10 μg/ml脂多糖的DMEM液培养6小时的加药组。

Methods: We divide the rats into 5 groups in random, with Morris method, detect the change of some active oxygen radicals such as super-oxide demitasse, Nitric Oxide Synthase, malondialdehyde etc. Also, we detect the change of cholinesterase, Monoamine Oxidize; using HE,PAS staining, immuno-histochemical technique, detect hippocampus CA1 cerebral pathology slices optical density value of NOS, CHE and lipofuscin of neural cell; detecting apoptosis rate and the expression of P53 , which are neuronal apoptosis related genes.

大鼠随机分为5组,采用"Morris水迷宫"法观察脑缺血性模型大鼠学习记忆功能,检测超氧化物歧化酶、一氧化氮合酶、丙二醛等自由基代谢异常的改变,检测胆碱酯酶、单胺氧化酶等老化相关酶的变化、脑组织神经细胞免疫组织化学技术、检查海马CA1区脑组织的病理切片,检测NOS、CHE光密度值;流式细胞技术:检测细胞凋亡率,及促细胞凋亡基因、P_(53)蛋白表达;病理切片采用HE染色、PAS染色及免疫组化法检查,检测对大鼠海马神经元细胞一般病理变化及脑细胞内脂褐含量。

Statistical analysis was performed to determine the relationship between staining of denture and the above ...

采用统计学方法,分析全口义齿着色与上述因素的关系。

RESULTS: After ischemia-reperfusion injury, the rats had hydrouria, urine osmotic pressure depress, symptoms of carnine and urea nitrogen increasing. HE staining demonstrated that renal tubular epithelial cells were swelling, necrosis, and desquamate. Aquaporin-1 expression and its mRNA level was decreased; in particular, the expression and level were the lowest at day 1 after ischemia-reperfusion injury and recovered to normal value at day 5 after ischemia-reperfusion injury.

结果:大鼠肾脏缺血再灌注损伤后出现尿量增多、尿渗透压降低,血肌苷、尿素氮升高症状;苏木精-伊红染色示肾小管上皮细胞肿胀、坏死、脱落;水通道蛋白表达量及其mRNA含量均较对照组减少,这些变化于缺血再灌注损伤 1 d时最低,至缺血再灌注损伤 5 d时恢复正常。

In scc-3 mutant animals, normal SCs were not visible and ~24 DAPI-staining positive structures were seen in diakinesis, indicating that SCC-3 is necessary for the establishment or maintenance of sister-chromatid cohesion.

在scc-3突变型线虫细胞中,无法观察到正常的联会复合体,且在终变期出现大约24个DAPI染色阳性信号。

In evl-14 mutant animals, synaptonemal complexes were detectable at the pachytene arrest, but more than the usual six DAPI-staining positive structures were seen in diakinesis, suggesting that EVL-14/PDS-5 is important for the maintenance of sister chromatid cohesion in the late prophase.

这一结果提示EVL-14/PDS-5对于在减数分裂的晚前期维持姐妹染色单体粘连是十分重要的。

Methods: Twelve microsatellite markers located at chromosomes 3p,9p and 14q were selected to investigate microsatellite alterations in 31 RCC specimens and their paired metastasis specimens by polymerase chain reaction-polyacrylamide gel electrophoresis-ethylene dibromide (PCR-PAGE-EB) staining and sequencing.

选取位于染色体3p、9p、14q上的共计 12个微卫星多态性标记,采用PCR-中性聚丙烯酰胺凝胶电泳-EB染色和测序的方法对31例肾细胞癌患者的原发病灶和配对的转移病灶进行MSI和LOH分析。

Methods: Twelve microsatellite markers located at chromosomes 3p, 9p and 14q were selected to investigate microsatellite alterations in 31 RCC specimens and their paired metastasis specimens by polymerase chain reaction-polyacrylamide gel electrophoresis ethylene dibromide (PCR-FAGE-EB) staining and sequencing.

选取位于染色体3p、9p、14q上的共计12个微卫星多态性标记,采用PCR-中性聚丙烯酰胺凝胶电泳-EB染色和测序的方法对31例肾细胞癌患者的原发病灶和配对的转移病灶进行MSI和LOH分析。

Some of the differential expression proteins were verified by Western blot analysis and immunohistochemical staining, and the results were consistent with 2-DE analysis.

一些差异表达的蛋白质通过Western blot分析和免疫组织化学染色进行了验证,结果和2-DE分析的相一致。

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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。

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。

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。