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phosphate相关的网络例句

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The LV messenger ribonucleic acid levels of contractile and calcium regulatory genes were measured by quantitative real time polymerase chain reaction and normalized for glyceraldehyde 3-phosphate dehydrogenase.

采用定量实时聚合酶链反应测定心室收缩蛋白和钙调蛋白基因信使RNA水平,采用3-磷酸甘油醛脱氢酶标准化。

The rabbits' RNA was extracted from the lavage cells, and mRNA for TNFα was quantitated by reverse-transcription polymerase chain reaction using glyceraldehyde 3-phosphate dehydrogenase as an internal standard.

第二部分:12只表面活性物质缺乏兔,以CMV(n=6)或PHY+PEEPi(n=6)通气1h后,重复灌洗,提取灌洗液中的兔RNA,以GAPDH为内参照RT-PCR的方法来定量分析TNFαmRNA。

Among the genes were glyceraldehyde 3-phosphate dehydrogenase, serine protease inhibitors, mitochondrion coding region, part of myosin heavy chain gene and two new genes, respectively.

结果 筛选出 6种蛋白分子基因:3-磷酸甘油醛脱氢酶,丝氨酸蛋白酶抑制剂,线粒体编码蛋白,肌球蛋白部分重链基因以及两个未知新基因。

Methods The total RNA of leucocyte was extracted 43 allergic vasculitis patients and 24 normal subjects before and after treatment with Trizol reagent and the integrity and concentrations of HLA-DRw53 gene mRNA were determined by agarose gel electrophoresis and UV spectrophotometer after denatured with 1% formaldehyde, the product was transcribed into complementary retroviral synthetic deoxyribonucleic acid, and sequence-specific primers were designed based on the sequences of second HLA-DRw53 gene exon and housekeeping gene glyceraldehyde phosphate-dehydrogenase cDNA.

利用随机引物逆转录合成互补脱氧核糖核酸,根据HLA-DRw53基因第二外显子序列和管家基因人磷酸甘油醛脱氢酶的cDNA序列设计序列特异性引物。检测43例变应性血管炎患者治疗前后与24名正常人HLA-DRw53基因mRNA表达量的变化。

Methods: Atrial tissue was obtained from the right appendage during open surgery in 25 patients with RHD. The mRNA of ACE and ERK2 and AT1R was semi-qualified by reverse transcription-ploymerase chain reaction and normalized to the glyceraldehyde 3-phosphate dehydrogenase. Western blotting analysis was employed to examine the expression of ACE and ERK and AT1R. Atrial collagen volume fraction was detected by Masson's stain.

25例风心病二尖瓣狭窄接受外科手术者,手术时取右心耳处心房组织500mg,通过逆转录—聚合酶链反应技术,以GAPDH为内参照测量ACE、AT1R、ERK2的 mRNA变化,用Western Blotting了解ACE、AT1R、ERK在蛋白水平表达的差异,经免疫组织化学了解胶原纤维容积分数改变情况。

Then folic acid targeted lipisome mediated MYCN siRNA(3.5mg/kg/day) was injected daily into tumor mass,continuously for 3 days, while same volume of normal saline, with the same protocol was injected in mice with control. Three hours after last day injection, all the mice were sacrificed, tumor mass was collected for MYCN and Glyceraldehyde phosphate dehydrogenase mRNA expression detection by real time RT-PCR.

剩余SCID鼠,实验组局部瘤组织中注射叶酸包裹脂质体MYCN siRNA,剂量为3.5mg/kg,每天一次,连续三天,空白对照组相同部位、相同时间注射等量生理盐水,末次注射3小时后脱臼法处死动物,取肿瘤组织,提取总RNA。

Its substrate is glycolate produced in C3 plants by the oxidation of ribulose bisphosphate to glycerate 3-phosphate and phosphoglycolic acid.

在过氧化物酶体中,乙醇酸在乙醇酸氧化酶作用下,被氧化为乙醛酸和过氧化氢。

Glyceraldehyde-3-phosphate dehydrogenaseis known for its pivotal role in glycolysisasa classical glycolytic protein in cytosolic energy production.

3-磷酸甘油醛脱氢酶作为一种糖酵解蛋白在糖酵解的能量产生中发挥着重要作用。

Glycerol obtained from the breakdown of fat is metabolized by conversion to dihydroxyacetone phosphate, a glycolytic intermediate, in two enzyme-catalyzed reactions.

来源于脂肪的甘油经两步酶促反应代谢转化为糖酵解的中间产物磷酸二羟丙酮。

The coordination of glucose, phosphate and reaction time has a decisive effect on gramme molecule change effiency of ATP. One gramme of fresh mycelia changes 75 M AMP into ATP under appropriate laboratory.

在试验中发现高浓度葡萄糖能推迟ATP累积高峰出现的时间;高浓度磷酸盐能促进磷酸化反应;葡萄糖、磷酸盐和反应时三者的配合关系对ATP克分子转化率影响较大。

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