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induced相关的网络例句

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Methods Quantitative immunoblot analysis was used to examine sIgE and tIgE level in 364 chronic eczema children. All subjects were tested for food-induced and airborne-induced allergens equally.

采用德国Mediwiss过敏原体外检测系统,应用免疫印迹定量法对364例慢性湿疹患儿进行血清特异性IgE和总IgE检测。

Reactive oxygen species causing DNA oxidative damage comes from two kinds of ways:one is from cellular normal physiological metabolism;the other is from outer environment.Redox-sensitive green fluorescent protein was expressed in Saccharomyces cerevisiae.Recombinant cells were evaluated in monitoring the changes in the redox state of living cells when challenged with toxicologically relevant metal ions NaAsO_2 or Pb(NO_3)_2 by measuring emission intensity at 510 nm with a Hitachi F6500 fluorescence spectrophotometer,roGFP expressed in yeast responded not only to typical membrane-permeant oxidants H_2O_2 and reductants DTT,but also to toxicological metal ion-induced intracellular redox changes in a dose-dependent manner.Moreover,exposure of yeast cells to NaAsO_2 or Pb(NO_3)_2 at concentrations that induced redox changes reported by roGFP caused up to 2~3 fold increases in DNA mutation frequency.This mutagenic effect was largely caused by oxidative stress since blocking the production of hydryl radicals with thiourea significantly reduced the mutation rate as well as delayed the cell death.

本文将对氧化还原状态变化敏感的绿色荧光蛋白roGFP1-R12,在酵母细胞中实现了多拷贝强表达;荧光扫描经强氧化剂H_2O_2和还原剂DTT以及环境中重金属NaAsO_2或Pb(NO_3)_2处理后的酵母细胞悬液,测定510 nm处的荧光发射强度结果显示,表达的绿色荧光蛋白对氧化还原水平敏感,且在510 nm处的荧光强度与一定的重金属浓度呈正相关,即roGFP1-R12在510nm处的荧光发射值随重金属浓度的增高而增强,从而说明重金属对细胞的毒性在一定程度上很可能是通过破坏细胞内的氧化还原平衡发生作用;同时通过该绿色荧光蛋白对胞内氧化还原状态变化的响应情况可以来实时检测环境中的重金属;遗传学的点突变频率及致死率实验数据表明,重金属能导致菌体的点突变频率和致死率升高,且活性氧的清除剂巯基脲能明显降低这种点突变和致死率,说明由重金属引发的这种点突变和致死效应在很大程度上是依赖于重金属对细胞诱导产生的氧化胁迫。

Calcium ionophore-induced tryptase release was inhibited 60% and 69% by 10 and 50 microM of DL, respectively, and anti-IgE-induced tryptase release was inhibited 33%, 47% and 66% for 1, 10 and 50 microM of DL.

研究发现浓度分别为1、10和50mM的DL分别使钙离子载体诱导的LTC4释放下降29%、35%和39%,分别使IgE诱导的类胰蛋白酶释放下降33%、47%和66%。

Effects of Simvastatin on the Transdifferentiation of Renal Tubular Epithelial Cells Induced with High Glucose UANG Xiao-xia,KE Chang-bin,ZHANG Qing-hong,ZHANG Jian-e*(Department of Nephrology;Department of Anesthesia,Taihe Hospital,Yunyang Medical College,Shiyan,Hubei 442000,China)Abstract:Objective To investigate the effects of simvastatin in renal tubular epithelial cells transdifferentiation induced with high glucose.

作者:黄晓霞,柯昌斌,张庆红,张建鄂*作者单位:郧阳医学院附属太和医院肾病内科;麻醉科,湖北十堰 442000 目的:观察辛伐他汀对高糖诱导的肾小管上皮细胞转分化的作用。

Two special TL phenomena have been found in Yanzhuang meteorite through the determination of the natural TL, annealed TL and induced TL by β radiation: l.when the sample of Yanzhuang meteorite is annealed at temperature up to 500℃, the TL peak induced by β rays moves to lower temperature with the increasing of irradiation dose; 2.when the annealed temperature is greater than 600℃, the TL peak temperature of the annealed sample is higher than that of the unannealed sample.

991年10月31日21点45分在广东省翁源县岩庄乡境内发生了陨石降落。从降落现场收集到3.skg的陨石样品,经初步鉴定为H6型、具有强冲击变质特性的珍稀普通球粒陨石。根据陨石命名规则定名为岩庄陨石。普通球粒陨石是目前研究太阳系早期所发生的化学与物理变化过程的最好的信息来源。

The HSS action showed a dose-effect manner and this action was proved uneffective with the larger dose of CCl〓.(2) Hepatic histological findings indicated that CCl〓-induced hepatic lesions could been alliviated by HSS.(3) CCl〓-induced reduction of hepatic mitochondrial succinic dehydrogenase activity was restored by the treatment of HSS.

相反,如果CCl〓所用剂量过大,HSS将无抗损伤作用;(2)HSS可使CCl〓损伤肝组织的程度减轻,用肝组织切片可充分证明这一现象;(3)HSS可使CCl〓损害肝细胞线粒体琥珀酸脱氢酶的活性恢复,用组织化学法可得到证实。

In this study, We used longer DD primers in combination with a two-step PCR protocol to overcome these two problems in term of modified methods of Martin and Pardee.K562 erythroleukemia cell differentiation induced by HEMIN or PMA for 36 hours was used as erythriod or megakaryocytic differentiation model in vitro.Total RNAs were extracted from induced and uninduced K562 cells and were applied to mRNA differential display analysis.

为解决此问题,我们参照Martin和Pardee的改进方案[3],建立了一种使用长引物,进行二步PCR的改进DDRT-PCR方法,以氯高铁血红素和肉豆蔻佛波酯诱导K562细胞36小时作为体外红细胞和巨核细胞分化模型,取诱导前后的细胞总RNA进行mRNA差异显示分析。

To get more information of the function of human Era on cell cycle, the complete control inducible mammalian expression system was used to express human Era mutant and analyzed cell cycle of uninduced (add 1% ethanol) and induced (10μM Pon A) cell lines by flowcytometer, the primary results demonstrated human Era mutant could inhibit apoptosis induced by ethanol, and Era S36N may stimulate the expression of Bcl-2 as detected by Western Blot.

在构建稳定高表达蜕皮激素受体基因的细胞株3V3的基础上,转染突变型人Era的表达载体进行压力筛选,对所得到的单克隆细胞株进行诱导与未诱导条件下细胞周期的分析,结果表明未诱导加酒精的对照细胞可以引起细胞凋亡,而Era诱导表达后可以显著抑制凋亡细胞的数量,Western表明Era S36N可以诱导细胞Bcl-2表达,提示人Era可能与细胞凋亡相关。

A 1: Uninduced supernant of cell lysate by sonication; 2: Induced supernant of cell lysate by sonication; 3: Uninduced precipitate of cell lysate by sonication; 4: Induced inclusion body of cell lysate by sonication; 5: Purified ULBP4 protein; M: Low molecular marker proteins.

2.3 体外NKG2D结合实验和细胞因子分泌实验间接ELISA检测结果显示:原核表达复性后的ULBP4能与人NKG2D结合,而带His标签的无关蛋白则不能与之结合,说明复性后的ULBP4仍能维持正确的天然构像。

ANP and CX43 began to express at 2nd week after induction and increased gradually,about 60% of the resulting myogenic cells were positive at 4th week after induction ,they were negative for uninduced cells.hMSCs'surface antigen profiles obtained by Flow Cytometry were negative for CD31\CD34\CD45 before and after induction,but CD90 expressed higher after induction while was weak positive before induction(P.05). Apotosis index was correlated with the cultural time after induction,The apoptosis rate of induced hMSCs was remarkably higher than control group(P.01),and the variation between groups was notable(P.05),the cell cycle analysis showed that the percentages of G_0/G_1phases were reduced significantly after induction. The expresstion levels ofβ-MHC and CTNT mRNA were undetectable before induction,began to increase at 1st、4th week after induction,reached the peak at 6th week and decreased after that,the expression of Bcl-2 and Bax mRNA varied regularly after treated with 5-azacytidine. hMSCs'resting membrane potential、range and rate of depolarization were heightened gradually after being induced.

结果:hMSCs诱导前为纺锤形,诱导后第2天部分细胞即开始发生形变,呈球形或短棒状,1周后胞浆中颗粒增多,约20~30%细胞边缘呈毛刷样变化;hMSCs表面抗原CD31、CD34、CD45在诱导前后差异无统计学意义,CD90未诱导时表达呈弱阳性,诱导后明显增高(P.05);ANP和CX43在诱导前无表达,诱导后第2周开始表达且表达随时间逐渐增强,但CX43在诱导后第5周表达量开始降低。hMSCs诱导后凋亡指数随诱导后培养时间增加,低浓度诱导组低于标准浓度诱导组,组间差异有统计学意义(P.05),G_0/G_1期细胞比例诱导后较对照组显著减少(P.05);β-MHC和CTNT基因分别在诱导后第1周和第4周时表达开始增强,在第6周时均达到高峰,第8周时表达开始衰减,Bcl-2、Bax基因表达呈时间依赖性变化,hMSCs经诱导后随心肌样细胞特征的表达膜静息电位、去极化幅值和去极化速率逐渐增高。

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