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Besides, HIF-1 can quickly induce a lot of expressions and the adjustment of anoxia-induced genes, so as to enhance the hypoxia-induced genetic transcription and increase the expressions, and engender physiological effects, such as adjusting the transcription of EPO genes to increase their production, thereby the red blood cells quantity is enlarged, which strengthens the ability of oxygen transportation and mitigates anoxia; adjusting VEGF genetic transcription to engender more blood capillaries, consequently the transportation and supply of oxygen and substance of energy source are strengthened; adjusting the glycolytic enzyme to enhance glycolysis ability under anoxemia condition and increase energy supply; functioning on HO-1 genes in vascular smooth muscle cells to produce HO-1, which can engender NO and CO as pneumatic signal molecules to activate the guanylate cyclases, thus CGMP level is improved to make the vascular smooth muscles chalasia, to restrain platelet agglutination, so that theblood flow and vascular permeability are increased, and the anoxic tissues obtain ample oxygen supply, etc..

在低氧环境中,HIF-1可以被很快诱导大量表达并介导低氧诱导基因的调控,使低氧诱导基因转录增强,表达产物增多,产生生理效应。

The profile of liver CYP450 induction by DEX in male rat After 4 daily i.p. administering of 0,25, 50 and lOOmg/kg/d DEX in male Wistar rat, it was determined the total CYP450 content, the mRNA and protein expression levels of CYP3A1, CYP3A2 and CYP2B1/2, and the ERD (CYP3A catalytic activity), PROD (CYP2B catalytic activity) and BROD (total CYP450 catalytic activity) in livers.

DEX对雄性大鼠肝脏CYP450的诱导效应雄性Wistar大鼠腹注0、25、50和100mg DEX/kg/d诱导处理4天后,测定大鼠肝脏总CYP450含量,CYP3A1、CYP3A2和CYP2B1/2的mRNA及蛋白表达水平,肝脏红酶素脱甲基酶(ERD,CYP3A活性),苄氧基试卤灵脱乙基酶(PROD,CYP2B活性),苯氧基试卤灵脱乙基酶(BROD,总CYP450活性),结果表明,CYP450含量、ERD、PROD和BROD在DEX多次诱导后都有升高,CYP3A1 mRNA表达水平、蛋白含量和酶活性有明显的升高,剂量效应关系明显;CYP3A2蛋白也有明显升高,而其mRNA表达水平却没有变化,提示CYP3A1和CYP3A2的诱导机制可能不同。

The profile of liver CYP450 induction by DEX in male ratAfter 4 daily i.p. administering of 0,25, 50 and lOOmg/kg/d DEX in male Wistar rat, it was determined the total CYP450 content, the mRNA and protein expression levels of CYP3A1, CYP3A2 and CYP2B1/2, and the ERD (CYP3A catalytic activity), PROD (CYP2B catalytic activity) and BROD (total CYP450 catalytic activity) in livers.

DEX对雄性大鼠肝脏CYP450的诱导效应雄性Wistar大鼠腹注0、25、50和100mg DEX/kg/d诱导处理4天后,测定大鼠肝脏总CYP450含量,CYP3A1、CYP3A2和CYP2B1/2的mRNA及蛋白表达水平,肝脏红酶素脱甲基酶(ERD,CYP3A活性),苄氧基试卤灵脱乙基酶(PROD,CYP2B活性),苯氧基试卤灵脱乙基酶(BROD,总CYP450活性),结果表明,CYP450含量、ERD、PROD和BROD在DEX多次诱导后都有升高,CYP3A1 mRNA表达水平、蛋白含量和酶活性有明显的升高,剂量效应关系明显;CYP3A2蛋白也有明显升高,而其mRNA表达水平却没有变化,提示CYP3A1和CYP3A2的诱导机制可能不同。

Result: The inductivity of leaves was the highest about 87.5%, followed with the stem section and leafstalk; The inductivity of nutrient medium such as MS, B5 callus was higher than the ones like H, SH and the White callus amended one; It was found that low-grade Phvalue benefits the growth of callus. The experiment result showed that different pH showed little difference in quality. The best condition of culture was 25 ℃in temperature. Conclusion: The best culture condition for callus was the leaves as explantation.

结果:叶片的诱导率最高,为87.5%;茎段次之,叶柄较差;培养基MS,B5愈伤组织诱导率较高,达到了80%以上,高于培养基H,SH和改良White的愈伤组织诱导率;偏低的pH对愈伤组织生长有利,出愈率高,但从愈伤组织生长质量方面看,不同pH差异不明显;愈伤组织诱导最适温度为25 ℃。

Result: The inductivity of leaves was the highest about 87.5%,followed with the stem section and leafstalk;The inductivity of nutrient medium such as MS,B5 callus was higher than the on...

结果:叶片的诱导率最高,为87.5%;茎段次之,叶柄较差;培养基MS,B5愈伤组织诱导率较高,达到了80%以上,高于培养基H,SH和改良W h ite的愈伤组织诱导率;偏低的pH对愈伤组织生长有利,出愈率高,但从愈伤组织生长质量方面看,不同pH差异不明显;愈伤组织诱导最适温度为25℃。

The results showed that BTH, SA, OAA and Na2SiO3 had significant induction effects, and the optimum concentration of four chemicals for resistance induction of melon against Erysiphe cucurbitacearum were 0.35, 1.0, 30 mmol/L and 10 mmol/L respectively.

各种诱导剂的最适诱导浓度分别为BTH 0.35 mmol/L、SA 1.0 mmol/L、OAA 30 mmol/L、Na2SiO3 10 mmol/L;适宜浓度下的诱导效果分别为:72.4%、49.9%、43.4%和34.9%。磷酸氢二钾(K2HPO4)在供试浓度范围内对甜瓜抗白粉病的诱导作用不显著。

This has been discussed before and demonstrated in previous studies but for e-antigen and in the surface antigen the hepatologist considers that they are very important in inducing the immune tolerance because this kind of antigen can induce the impairment of dendritic cells and also can induce the generation of regulatory T cells.

HBeAg在诱导免疫耐受方面的作用已经被讨论过并在以前的研究中证明过,现在肝病学家认为HBsAg在诱导免疫耐受方面也有重要作用,因为这类抗原能诱导树突状细胞的损伤,并能诱导产生调节性T细胞。

The most of the product became soluble from inclusion body by lowering induction temperature. At the same time the gene was cloned into vector pMAL-p2X, which was translated in E. coli TB1 and expressed a fusion protein. We optimized the induction time and achieved high expression. But there was no obvious product secreted in the periplasm extract. Almost all fusion protein is expressed soluble in cytoplasm.

利用融合型表达载体pTYB11-EFE融合型表达,对诱导剂IPTG的浓度和诱导温度进行了优化,通过降低诱导温度使产物由包含体变成可溶性融合型产物;利用融合型分泌表达载体pMAL-p2X构建了表达载体pMAL-p2X-EFE-7~#,对诱导时间进行了优化,获得了较高的表达量,但发现产物没有明显的分泌表达,绝大部分是以可溶形式存在于胞内。

METHODS: Bone marrow was sterilely separated from human. After heparinization, human BMSCs were harvested using density gradient centrifugation and adherence method. At the fifth passage, BMSCs at 1×108/L were incubated in the 6-well plate and divided into 2 groups. BMSCs in the edaravone group were 50% confluent and incubated in L-DMEM containing basic fibroblast growth factor and fetal bovine serum for 24 hours. After washing in PBS, these BMSCs were incubated in serum-free L-DMEM containing 20 mg/L edaravone for 24 hours. BMSCs in the blank control group were incubated in L-DMEM, supplemented with 10% fetal bovine serum.

无菌抽取的骨髓经肝素化后,采用密度梯度离心法及贴壁筛选法分离获得人骨髓间充质干细胞,传至第5代按1× 108 L-1接种于6孔板内,设立2组,依达拉奉组细胞达50%融合时用含碱性成纤维生长因子、胎牛血清的L-DMEM预诱导24 h,PBS洗涤后再用20 mg/L依达拉奉无血清L-DMEM诱导24 h;空白对照组始终用含体积分数为10%胎牛血清的L-DMEM培养,不加任何预诱导剂和诱导剂。

METHODS: Normal human BMSCs were isolated and cultured by the whole bone marrow method. Cells of the third passage at 1×108/L were incubated on coverslip in a 6-well plate, and randomly divided into 3 groups: osteogenic induction group, which was added with primary medium and osteogenic inducer, supplemented with 10-8 mol/L dexamethasone, 10 mmol/L β-phosphoglycerol and 50 mg/L vitamin C; leptin osteogenic induction group was added with 50 nmol/l leptin in addition to osteogenic inducer. Cells in the blank control group were only treated with LG-DMEM containing 10% fetal bovine serum.

采用全骨髓法体外分离培养人骨髓间充质干细胞,传至第3代以1×108 L-1密度接种至预置盖玻片的6孔培养板中,设立3组:成骨诱导组添加原代培养液后,再加入含10-8 mol/L地塞米松、10 mmol/L β-磷酸甘油、50 mg/L维生素C的成骨诱导培养基;成骨+瘦素诱导组添加成骨诱导培养基后,再加入50 nmol/L瘦素;空白对照组仅加入含体积分数为10%胎牛血清的LG-DMEM培养液。

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