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免疫化学

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Methods Establishing a model of whole cerebral ischemia-reperfusion in rats; examining the expressions of TrkA and NGF on cochleas assuming the method of immunohistochemistry stain; and examining the time and distribution of the cochlear hair cell apoptosis through the terminal deoxynucleotidyl transferasemediated dUTP nick end labeling.

建立大鼠全脑缺血再灌注模型,采用免疫组织化学染色方法检测TrkA和NGF在耳蜗中的表达;用TUNEL法检测耳蜗毛细胞发生凋亡的时相和分布。

The percentage of ERa was approximately 24% in the anterior pituitary gland of adult chicken, and there was no significant difference between laying hens and adult cockerels.

免疫组织化学双标记的结果证明,ERα在成年鸡垂体中所表达的细胞类型主要是LH细胞,而产蛋母鸡中双标记细胞显著高于成年公鸡。

MAIN OUTCOME MEASURES: At 3, 7, 14, 28 days after the application of traction and 3, 7, 14, 28 days after the removal of traction, the expression of receptor activator of nuclear factor κB ligand/osteoprotegerin in the subchondral bone of the bilateral condyles was analyzed by semi-quantitative immunohistochemistry.

主要观察指标:加力3,7,14,28 d及撤除外力后3,7,14,28 d,以免疫组织化学半定量检测双侧髁状突软骨下骨中核因子κB受体活化因子配基/骨保护素表达。

After renal cortexes were Grinded and digested with 0.25%tryspase.The cell types of epithelial cell were identified by immunocytochemistry.The injury model of rats, renal tubular epithelial cells were established by using gentamicin.And observed the role of bFGF in renal tubular epithelial cell.

通过对大鼠肾皮质研磨、过网的方法,并以0.25%胰蛋白酶消化,以免疫细胞化学方法鉴定体外培养的肾小管上皮细胞(抗Cytokeratin 18抗体),以庆大霉素对培养的肾小管上皮细胞建立损害作用模型,然后观察碱性成纤维细胞生长因子对损害的肾小管上皮细胞的保护作用。

After 3-8 passages, the oral CAFs and the normal mucosa fibroblasts from tissue culture were observed under light microscope. Vimentin,α-SMA and Cytokeratin protein were detected by immunohistochemistry SP method on glass coverslips. VEGF, TGF-β1, MMP-9, Tenascin-C mRNA were analyzed by semi-quantitative RT-PCR.

用组织块培养法获得原代CAFs和正常粘膜成纤维细胞,0.25%胰蛋白酶消化传代和纯化细胞;通过形态学观察和免疫细胞化学染色对口腔CAFs和NMFs进行鉴定:采用半定量RT-PCR检测口腔CAFs和NMFs 4种基因的表达。

Results:The positive expression of P53 and c-Myc protein in nuclei was bound up with poor-differentiated tumours;the positive expression of Fas and c-Myc protein in cytoplasms was consistent with well-differentiated tumours.

采用免疫组织化学方法对骨肉瘤、骨化性纤维瘤、骨纤维结构不良和正常骨痂组织进行c-Myc、Fas和P53蛋白测定,与肿瘤组织学分级、细胞分化及核丝分裂比较分析。

Methods: Neuroepithelial stem cells derived from the embryonic neural tube of GFP transgenic mice were cultured and depurated in free serum medium containing B27, bFGF and EGF, and then they were directionally transplanted into the striatum of rats.

将GFP转基因鼠的胚胎神经上皮干细胞置于无血清培养基内纯化扩增,用巢蛋白免疫组织化学染色鉴定神经干细胞,将扩增后的含GFP基因的神经干细胞在立体定位仪下,定向移植到大鼠的纹状体内。

Articular cartilage of femur head epiphyses was collected in 3,6,12,24,48 hours,5 days,2 and 4 weeks after the operation.Expression of iNOS and HSP70 were analyzed by immunohistochemical technique.

制作4周龄SD大鼠缺血再灌流及对照模型,每组各40只,于术后3、6、12、24、48h、5d、2、4周不同时点对股骨头骨骺关节软骨iNOS及HSP70进行免疫组织化学检测。

Mechanical strains also regulated the protein and mRNA expression of several differentiation markers, as well as the activation of extracellular signal-regulated kinases, p38 MAP kinase and protein kinase B in a frequency-dependent manner. Furthermore, the inhibition of p38 pathway could block the strain-frequency induced the phenotype modulation of VSMCs, neither ERKs nor Akt. Frequency of mechanical strain, not conditioned medium, regulated the phenotype of VSMCs in a frequency-dependent manner. Rho-GDI alpha was suppressed by the mechanical strain at 1Hz.

采用免疫细胞化学法检测VSMCs形态和排列的变化;RT-PCR和Western blotting检测表型标志分子α-肌动蛋白、肌球蛋白重链(SM1/2)、肌动蛋白相关蛋白SM22α和调宁蛋白(h1-calponin)的mRNA和蛋白水平的变化;抑制剂或RNA干扰阻断可能的信号调节分子的活性或表达,包括p38、细胞外信号调节激酶1/(2extracellular signal-regulated kinases, ERK1/2)、蛋白激酶B和Rho-鸟苷酸解离抑制因子(Rho-guanine nucleotide dissociation inhibitor, Rho-GDI alpha),研究了不同频率张应变对VSMCs表型转化的影响及其调节机制。

Immunohistochemistry were positive for CD34 in some region where the fibroblast actively proliferated, whereas fibrocytes in mature fibrous tissue were negatively stained.

CD34免疫组织化学染色显示一些增生活跃的纤维母细胞明显表达CD34,成熟的纤维组织内的纤维细胞CD34则为阴性。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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