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Bax相关的网络例句
与 Bax 相关的网络例句 [注:此内容来源于网络,仅供参考]

However, a steady input of evidence for the transcription-independent function of p53 in apoptosis has been accumulating recently. Although a detailed mechanism has not yet been determined, recent data have revealed that upon an apoptotic stimulus, p53 translocates into mitochondria to interact directly with Bcl-2 or Bcl-xL to displace and activate proapoptotic Bax signaling.

但是,还有研究证明p53也通过转录非依赖的形式来调节细胞凋亡,尽管这个作用的机制还没有被详细的阐明,但是最近的研究报道说明了,p53可以直接转移定位到线粒体上,与Bcl-2或者Bcl-xl结合后,从而使Bax游离下来并活化。

Control group was also set up.Then the AO/EB fluorescence double-dye technique,immunocytochemistry staining,Fluo-3 staining and Rhodamine 123 uptake assay approaches were adopted to observe the apoptotic rate,expression levels of Bcl-2 and Bax proteins,concentration of cytoplasmic free Ca2+ and mitochondrial transmembrane potential of NCI-H460 cells.

采用AO/EB荧光双染、免疫细胞化学染色、Rhodamine 123摄取法及Fluo-3/AM染色分别观察NCI-H460细胞的凋亡、Bcl-2及Bax蛋白的表达量、线粒体跨膜电位及细胞内游离钙离子浓度。

Methods: The immunohistochemical method was used to detect the expressions of apoptosis related proteins Bcl-2, Bax and myoglobin in the autopsied hearts of sudden coronary death, AMI and non-cardiac death in 20 cases respectively.

应用S-P免疫组化方法及图象分析技术检测Bcl-2、Bax及Mb在SCD、AMI及非心脏原因死亡的人尸检标本各20例中的表达情况。

We intend to detect the expression of apoptosis related proteins Bcl-2, Bax and myoglobin in the autopsied hearts of sudden coronary death and acute myocardium infarction in order to find some sensitive, reliable markers for the forensic diagnosis of SCD and early AMI.

本实验拟用免疫组化的方法检测凋亡相关蛋Bcl-2、Bax及心肌结构蛋白肌红蛋白(myoglobin,Mb)在早期心肌缺血性损伤中的表达情况,从而为SCD和早期急性心肌梗死(acute myocardium infarction,AMI)的诊断提供灵敏、可靠的辅助诊断指标。

Bcl|2 and bax were studied by strept Avidin|Biontin Complex immunohistochemistry.

目的 探讨端粒酶检测在乳腺癌诊断中的作用及其在乳腺癌发生中与bcl|2和bax蛋白表达的相关性。

Methods With in situ hybridzation to detect the expression and activity of telomerase. bcl|2 and bax were studied by strept Avidin|Biontin Complex immunohistochemistry.

用原位杂交方法检测端粒酶的表达及其活性,采用免疫组织化学技术SABC法检测bcl|2和bax。

Bcl|2 and bax were studied by strept avidin|biontin complex immunohistochemistry.results the expression rate of telomerase in breast cancer was significantly higher than that in precancerous breast(p<0.01) and in breast benign tumors.

用原位杂交方法检测端粒酶的表达及其活性,采用免疫组织化学技术sabc法检测bcl|2和bax。结果端粒酶在乳腺癌中的表达率明显高于癌前病变(p.01)和乳腺良性肿瘤。

Cerebral cortexes were removed and then dissociated, measured with flow cytometer analyze cell apoptosis, the morphological changes were examined by electron microscope.(2) Measured cell apoptosis of cerebral cortexes with TUNEL.(3) detected expressions of Bcl-2, Bax and Caspase-3 proteins with the technique of immunohistochemistry.

1取大脑皮层细胞制成细胞悬液,流式细胞仪分析细胞凋亡改变,电镜观察细胞超微结构的变化;(2)用原位缺口末端标记法检测凋亡细胞百分率;(3)免疫组化法检测Bcl-2、Bax和Caspase-3蛋白表达。

Forty SD female rats were divided randomly into four groups : control (received normal saline, CTX, S1P+NS, S1P+CTX respectively. All rats were killed between the first and the second week in the diestrus stage after stopping medicines to compare the number of the primordial follicles,the primary follicles and the growth follicles. The expression of the Bcl-2 and Bax mRNA in the ovaries were examined by the RT-PCR.

40只雌性SD大鼠随机分为4组,即实验对照组、CTX组、 S1P+ NS组及S1P+CTX组,每组10只,于结束用药的第1~2周内的动情间期处死,观察卵泡数量的变化,并采用半定量RT-PCR检测卵巢组织Bcl-2及Bax 的mRNA变化。

Methods Cells were maintained in DMEM medium with 10% fetal bovine serum. Five days before the beginning of experiments, the cells were seeded in phenol red-free DMEM medium containing 5% charcoal dextran-treated FBS. The cells were harvested, and seeded in 6-well culture plates or in 75ml flacks. After NP, BisA and DBP treatments for 72h, the cells were harvested, and mRNA and protein expression of PCNA, bcl-2 and bax were detected by reverse transcription-polymerase chain reaction and immunohistochemistry, respectively.

方法]T47D细胞在含10%胎牛血清的DMEM培养液中进行常规传代培养,实验前将细胞转移至无酚红DMEM(含5%活性碳葡聚糖苷处理过的FBS)中继续培养5d,收集细胞,PBS洗涤后接种於内置盖玻片的6孔板或75ml培养瓶中,用32×10^(-7)mol/L NP、32×10^(-7)mol/L BisA及32×10^(-6)mol/L DBP对细胞分别处理72h,用半定量RT-PCR技术观察这3种化合物对核增殖抗原PCNA、bcl-2及bax mRNA表达的影响,并用免疫组化方法对结果进行验证。

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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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