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expressed相关的网络例句

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与 expressed 相关的网络例句 [注:此内容来源于网络,仅供参考]

Methods: Immunohistochemistry and image analysis techniques are applied to examine the phosphorylated extracellular signal-regulated kinase in epidermis of non-expanded skin and expanded skin. Results:Phosphorylated ERK expressed in basal cell layer of epiderm including non-expanded skin and expanded skin are expressed. But in expanded skin they are expressed significantly and densely compared to non-expanded skin. There are significant difference in relative to location of expanded skin and regions of expanded skin.

结果: 1扩张皮肤和正常皮肤表皮基底层都有磷酸化ERK 的表达和分布,但扩张皮肤中的磷酸化ERK的分布和表达较明显,染色较深且密,部分阳性细胞呈多层排列,有散在的增殖团区;2扩张皮肤的顶部和侧部差别不十分明显,而侧部和顶部与基底部有一定的差别,基底部染色较深,多为细胞核着色;3 经图像分析不同部位的正常皮肤和扩张皮肤以及扩张皮肤的不同部分的相对灰度值和阳性细胞密度,进一步证实了上述观察结果。

Was simultaneously injected into cisterna magna at the second injection blood in the presence of subarachnoid blood. At 2 to 4 days, GFP was expressed in leptomeninges over the brain stem, cortex and cerebral arteries, smooth muscle cells of small vessels were occasionlly transduced. GFP was expressed in adventitia of spastic basilar artery on days 2 (day 5 after first injection blood) after injection 〓, but was undetectable by days 4, transgene was not expressed in medial or intimal layers. The prensence of subarachnoid blood can not prevent access of adenovirus to vessels and transgene expression.

注入腺病毒载体后2天(初次注血第5天)行荧光显微镜、免疫组织化学和RT-PCR检测,结果在颅内大血管如基底动脉的外膜可见外源基因的表达,而外源基因不能转移至血管中膜和内膜,4天时(初次注血第7天)基底动脉的外膜中外源基因表达消失;注入腺病毒载体后2~4天,外源基因可以有效转移至颅底软脑膜细胞,小血管外膜和平滑肌层也可见外源基因的表达,表明蛛网膜下腔内的血凝块不能阻止腺病毒载体介导外源基因转移至颅内血管。

With the inducing time prolonged, the amount of fusion protein increased, and the highest content amounted to 39. 14% of total protein. Different temperature (15℃, 25℃ and 37℃) could induce expression of fusion protein, and the higher inducing temperature was, the more total fusion protein and soluble fusion protein was produced. Most fusion protein was expressed in the cytoplasm and was soluble, a little of fusion protein was expressed in periplasm or expressed as inclusion bodies, and no fusion protein was found in culture. Furthermore, the results of in vitro enzymatic reaction suggested that the fusion protein could catalyze the methylation of theobromine.

随着诱导时间的延长,表达的融合蛋白产量逐渐增加,表达蛋白总量最高可达到菌体总蛋白的39.14%;在15℃、25℃和37℃三个不同的诱导温度下,均能诱导产生融合蛋白,而且产生的融合蛋白的总量及其可溶性部分所占比例均随诱导温度升高而增加;在菌体的各个部位中,融合蛋白主要在细胞质中以可溶的形式进行表达,有少量在外周质中表达或以包含体形式在细胞质中表达。

Three genes specified expressed in hybrids and one gene over-expressed in hybrid were found. By cloning, sequencing and BLAST analysis, one specific expression cDNA band was cytosolic isocitrate dehydrogenase gene, the other two were new genes which function were unknown, and the over-expressed cDNA band was proteosome subunit p112 gene.

发现了 3 个杂种鸡特异表达的基因和 1 个杂种鸡表达增强的基因,进一步克隆、测序和比对分析初步表明:杂种特异表达的 cDNA 片断分别为鸡细胞质异柠檬酸脱氢酶基因和 2 个未知功能的新基因;杂种表达增强的 cDNA 片断为鸡蛋白酶体亚基 p112 基因。

The present results showed that both cytoplasm and membrane of neuronal soma and dendrite expressed NKCC1, while KCC2 only expressed in membrane of soma and dendrite. The results also indicated that the dendrites rather than the somata of neurons expressed more NKCC1 in adult rat neocortex, while the level of KCC2 expression in the dendrite membrane was similar to that in the membrane of somata.

结果显示:成年大鼠皮质神经元的胞浆和细胞膜均有NKCC1的表达,而KCC2主要表达在神经元胞体和树突膜上,其中NKCC1在神经元树突上的表达水平比胞体高,而KCC2的表达水平在树突和胞体膜上没有明显差异。

The inner ear expressed a tissue-specific splicing isoform of α1D, and that the cell line constantly expressed this isoform can be used in physiologic and pharmacologic researches of L-type voltage-gated Ca2+ channel expressed in cochleae.

内耳毛细胞表达组织特异性的α1D剪切异构体,该异构体在外源表达系统中的表达为今后研究耳蜗α1D L-型钙通道蛋白的电生理和药理特性奠定了基础。

All polarities must be expressed, and if they are not expressed in physicality, then they will be expressed in parallel lives.

所有极性必须被表达,如果它们没在物质层被表达,就会在平行生命中被表达。

Hass-PBP、Hass-GOBP-1、Hass-GOBP_2 genes were only expressed in the antennae of adult,but not in the other parts of body,which including proboscises,head without antennae,thorax,abdomen,leg,wing;besides,Hass-PBP gene was only expressed in the antennae of male adult,while Hass-GOBP_1、Hass-GOBP_2 genes were expressed in the antennae both of male and female adult.

烟夜蛾3种气味结合蛋白基因的时空表达:(1)烟夜蛾Hass-PBP、Hass-GOBP_1、(来源:A3cBCfc6c论文网www.abclunwen.com)Hass-GOBP_2基因在卵期、幼虫期、蛹期均不表达,只在成虫期表达,且表达量与成虫的日龄无关。

The results of in situ hybridization showed that the gene of Mdde was expressed mainly in epidermis of the body wall and fat bodies, and no expression signal was detected in tracheae, intestine and musculature. The gene of Mdde in epidermis expressed both in challenged larva and no-challenged larva, whereas the gene of mdde in fat body expressed only in challenged larva.

原位杂交的结果表明:Mdde基因在家蝇幼虫体内主要表达于表皮和脂肪体,在气管、肠和肌肉组织中没有检测到Mdde基因的表达;表皮中Mdde基因在微生物刺激前后均有表达,而脂肪体中Mdde基因经微生物刺激后才表达,刺激前不表达。

Expression patterns of genes differentially expressed in starch metabolism and cell cycle during endosperm development7 DAP kernals, 15 DAP endosperms and 25 DAP endosperms of B73, ae/wx and sh1 were used to study the expression patterns of 18 differentially expressed genes in sugar metabolism and 9 differentially expressed genes in cell cycle. We found that the expression patterns of Pul, SBEⅡa, UGPase, SUS3, SSⅡa in sh1 and Sh2-1, SUS3, SSⅡa in ae/wx were altered, revealing that these genes may interact with each other.

碳水化合物代谢基因和细胞周期基因随胚乳发育的变化以B73、ae/wx、sh1授粉后7天种子、15天和25天胚乳为材料,分析18个糖代谢差异基因和9个细胞周期调节相关的差异基因的表达模式,研究发现sh1突变体中Pul、SBEⅡa、UGPase、SUS3和SSⅡa基因表达模式发生改变,ae/wx突变体中Sh2-1、SUS3和SSⅡa基因表达模式发生改变,揭示了突变体对这些基因的巨大影响,反映了它们可能存在相互作用。

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