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expression error相关的网络例句

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PartⅠ The Expression and Location of HCK Gene During the Development of Rattus Heart Objective To investigate the mRNA expression of HCK gene in the developing rattus heart and to analyze the relationship between HCK gene expression and the heart development.

目的检测HCK基因在大鼠胚胎心脏发育过程中mRNA表达的变化,分析其与心脏发育的关系。

The ability to modulate the expression of multiple genes by tetracycline and its derivatives is likely to regulate the timing and level of gene expression, quantitatively induce the expression of toxic protein, increase therapeutic efficacy and safety, and provide a safe and regulatable way for gene therapy.

CHO-Tet-On细胞株的建立,可利用四环素及其衍生物调节多种外源基因的表达,有效调控基因表达的时间和水平,定量诱导毒性蛋白的表达,增加治疗的疗效和安全性,有望为基因治疗提供一条可控的安全途径。

Egr-1 mRNA and Egr-1 protein hadn't been found in the normal vein. The expressions of Egr-1 mRNA and Egr-1 protein had biphasic changes. By reverse transcription-PCR and in situ hybridization, we found that the level of Egr-1 mRNA rose at 1 hour after graft, the expression of Egr-1 mRNA was (35±7)%. Decline at hour 6, 24 and day 3, the positive rates of Egr-1 mRNA were (8±2)%,(8±6)% and (8±4)% respectively. Reincrease at day 7, a peak at day 28, the positive rate of Egr-1 mRNA was (45±6)%(compared with other phase, P<0.01). At day 42, the expression of Egr-1 mRNA declined again. Immunohistochemical staining and Western blot revealed Egr-1 protein had expressed at hour 2 early phase, the expression of Egr-1 protein was (30±5)%, and until to hour 6. The level of Egr-1 protein was decrease at hour 24 and day 3, the positive rates were (7±3)% and (7±8)% respectively.

结果 自体静脉移植后,Egr-1 mRNA和Egr-1蛋白的表达呈双相变化,即移植后1 h, Egr-1 mRNA表达迅速升高,阳性率为(35±7)%,6 h、24 h及3 d时下降到较低水平,阳性率分别为(8±2)%、(8±6)%和(8±4)%,7 d时又再升高,28 d时达高峰,阳性率为(45±6)%,此与其余各时点比较差异均有统计学意义(P<0.01),42 d时,Egr-1 mRNA的表达再次下降;移植早期(2 h)即有Egr-1蛋白的表达,阳性率为(30±5)%,并持续至6 h,24 h~3 d表达下降到较低水平,阳性率分别为(7±3)%和(7±8)%,7 d时又再升高,至移植后28 d,Egr-1蛋白的表达阳性率达到高峰,为(40±9)%,此与其余各时点比较差异有统计学意义(P<0.01)。

Two relevant sites of enzymatic digestion were added to the mTNF-α by PCR. The mTNF-α was linked to the 3'end of m/〓 in pGEX4T-1 vector. The prokaryotic expression vector pGEX4T-1m/〓-mTNF-α was constructed successfully. After induction and expression by IPTG, the expression of two kinds of fusion protein is 15% and 12% of total bacteria proteins respectively. The anti-HCC bifunctional antibodies m/〓-mTNF-α were identified by electrophoresis after the inclusion bodies were purified, denature, renature, re-purified, digested by thrombin and further purified.

采用PCR的方法在mTNF-α的两端加上所需要的酶切位点,将之连接在m/〓的3'端,构建原核表达载体pGEX4T-1 m/〓-mTNF-α,通过IPTG的诱导表达之后,两种融合蛋白的表达量分别占细菌总蛋白的15%、12%,表达产物经包涵体的纯化→变性→复性→纯化→凝血酶酶切→进一步纯化后,可以得到纯度为电泳纯的m/〓-mTNF-α抗肝癌双功能抗体。

BMP-7 expression was lower markly in Lung-kidney Qi Deficiency 、Liver-kidney yin Deficiency、 Qi-yin asthenia、Speen –kidney Yang Deficiency than normal control. BMP-7 expression decreased with Lung-kidney Qi Deficiency 、Liver-kidney yin Deficiency、 Qi-yin asthenia、Speen –kidney Yang Deficiency.It shows that the level of BMP-7 expression may play a role in Zheng differentiation-classification of TCM of the chronic glomerulonephritis.

中医证型与肾间质纤维化程度显著相关,肺肾气虚、肝肾阴虚型纤维化程度最轻,气阴两虚型其次,脾肾阳虚型纤维化程度最重,提示传统中医辩证分型与纤维化程度有关,在一定程度上可以反映慢性肾小球肾炎组织学损伤程度,肾间质纤维化程度可作为中医临床辨证参考依据。

The expression changes of TNF-α and p65 mRNA expression were detected by reverse transcription-polymerase chain reaction, the TNF-α level in the supernatant was determined by ELISA, and the expression of p65 in AR42J cell lines was detected by Stept Avidin-Biotio Complex.

逆转录-多聚酶链反应半定量法观察肿瘤坏死因子/p65亚单位mRNA表达的变化;ELISA法检测TNF-α在细胞上清中质量浓度的变化;链酶亲和素-生物素-过氧化物酶复合物法检测p65蛋白在AR42J细胞中的表达。

Objective This study was performed to observe the effect of microvascular density,and the expression of MMP-2/TIMP-2 in the subendocardial myocardium of DOCA-salt Hypertensive Rats left ventricle under the intervention of bosentan,and to evaluate the signifance of expression of MMP-2/TIMP-2 and the role of endothelin-1 on the expression of MMP-2/TIMP-2 in DHR heart.

目的探讨基质金属蛋白酶-2(MMP-2)在脱氧皮质酮-盐型高血压大鼠心脏微小血管重塑中作用及其可能的调节机制。

The protein had the same antigenicity as IgG, and the change of the protein had the same tendency as SHP-2, which was higher in canceration groups than in uncanceration groups and control groups in thymus cells, but there weren't significant change in bone marrow cells;⑧ The change law of the expression of SHP-1 and SHP-2 during γ-ray induced malignant transformation in BEAS-2B cell is that the expression of SHP-1 was increased synchronistically with malignant transformation of cell, and the expression of SHP-2 didn't have significant correlation with malignant transformation of cell.

癌变组胸腺细胞中SHP-2 mRNA编码PTPase催化区的700~1096bp间可能出现甲基化;⑦癌变组的胸腺细胞中存在一相对分子质量约为55×10〓的蛋白质,它与IgG具有相同的抗原性,其表达量的变化趋势与SHP-2的蛋白表达变化趋势基本一致,即在胸腺细胞中明显高于对照组及未癌变组,但在骨髓细胞中对照组高于癌变组;⑧SHP-1、SHP-2在γ射线诱发的BEAS-2B细胞恶性转化过程的变化规律:SHP-1蛋白表达量的升高与细胞的恶性转化在时间上基本一致,而SHP-2蛋白表达量与恶性转化无明显关系。

To test the hypothesis, neontal rat cadiomyocytes Treat with heat shock(HS,42℃,2h) to induce the expression of HSP70,then teated with 0.5mmol/L H2O2. We first found H2O2 can reduced cadiomyocytes apoptosis and HSP70 only over-expression in the HS group, other two group only express HSP70 a little in the test of expression of HSP70.Then we tested the concentration of Ca2+, the [Ca2+ ] of CON was 192.224+6.654, the [Ca2+ ] of H2O2 group was 290.6918+8.922and the [Ca2+]of HS group was 214.2633+4.484.To further determine how HSP70 repaired the Ca2+ homestasis, we measured calcium transient of each group.

实验中应用MTT和流式细胞技术检测细胞的凋亡,发现损伤组的存活率明显低于其他2组,热休克组(Heat shock group,HS group)细胞存活率略低于正常组细胞;免疫组化结果表明只有在HS组才检测到阳性反应,即是HSP70的表达,其他2组均为弱阳性结果;应用离子成像技术对细胞内钙离子浓度进行测定,发现损伤组290.6918+8.922明显高于正常组192.224+6.654和HS组214.2633+4.484,HS组细胞内的钙离子浓度略高于正常组;为了进一步探讨HSP70对于ROS引起的心肌凋亡过程中钙离子的调控机制,又对各组的心肌细胞进行了钙瞬变的测定。

This implies that DNA methylation of promoter exon 1_7 may not underly the mechanism of GR up-regulation in GLP-1 -programmed rats.5 Hippocampal expression of GLP-1R and NGFI-A mRNAHippocampal GLP-1R (p =.009) and NGFI-A (p =.001) gene mRNA expression were significantly up-regulated in GP group as compared to VP group.Taken together, neonatal intramuscular injection of plasmid DNA encoding GLP-1 affects behavior and hippocampal GR expression in adolescent rats.

提示GR exon 1_7启动子区域DNA甲基化可能不参与GLP-1导致的GR转录上调。6海马GLP-1R和NGFI-A mRNA表达GP组大鼠GLP-lR(P=。009)和NGFI-A(P=。001)表达均显著高于VP组,表明肌肉注射GLP-1可能通过作用于其海马受体提高NGFI-A表达,进而调控GR表达。

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