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

50Mmol/L NaCl stress had no influence on level of ATP in root of Ginkgo andAilanthus.Level of ATP in roots of Ginkgo,Ailanthus and Robinia decreased greatly under200mmol/L NaCl stress.The extent of decrease of ATP level accord to plant salt tolerance:Ginkgo is more salt tolerance,and ATP decreases more slowly than that of Ailanthus andRobinia.

11.50mmol/L的NaCl胁迫没有引起银杏和臭椿根尖ATP水平的明显改变;200mmol/L的NaCl胁迫引起银杏、刺槐和臭椿ATP水平指数性的衰减,ATP的下降幅度的变化与植物耐盐性一致:耐盐性强的银杏,ATP的下降幅度明显比刺槐和臭椿小。

FITC can inhibit the antimonite-stimulated ATPase activity of ArsA and a combination of ATP and antimonite can completely protect ArsA from the inactivation of FITC. The Lys residue in the glycine-rich loop in ArsA is possibly one of the sites for FITC modification. Antimonite can induce the fluorescence resonance energy transfer between FITC and TRITC that separately labeled on different ArsA molecules.

研究还发现FITC对ArsA的ATP酶活性有抑制作用,ATP和SbO〓与ArsA的结合完全拮抗这种抑制,说明ATP和SbO〓与ArsA的结合能够引起ArsA产生一种完全不同于它们单独与其结合时的构象变化,从而使ArsA上FITC的修饰位点变得不易接近,同时ATP结合位点内的Lys可能是FITC在ArsA上的结合位点之一。

Methods: In accordance with conventional reporter gene analysis reagent preparation method, the main component Luciferase, Luciferin and ATP were serial diluted to find the optimal concentration; Reaction solution was prepared according to the optimal concentration of the main component, then ATP were serial diluted to measure their reporter gene. Then standard curve of ATP were drawed. Tumor cell lines H1299 were serial diluted and their ATP were measured by reaction solution prepared to analyse the minimum cell number.

按照常规报告基因分析试剂配制方法,将其中主要成分Luciferase和Luciferin及ATP浓度进行倍比稀释后找到最适合反应的最佳浓度值;按照最佳浓度配制反应液,将ATP浓度倍比稀释测定报告基因数值并绘制标准曲线,分析检测灵敏度;另外选取肿瘤细胞株H1299,倍比稀释后裂解细胞应用配制好的反应液进行ATP检测,分析最低检测细胞数。

Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有按摩明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数按摩明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

Methods Cell culture,flow cytometry,HE staining,Nigrosine staining and electron microscopy were used. Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

Results: The light microscope pictures of group A(no [α-32P] ATP in the perfusate) showed that there was no specially labeled silver pellet in or out of rat liver cell. But the light microscope pictures of group B (37 MBq [α- 32P]ATP in the perfusate) showed that distribution of numerous [α-32P]ATP autoradiographic silver pellets in rat liver cell, and no autoradiographic silver pellet was found in the hepatic sinus and vessel.

结果:灌流液中不加[α-32P]ATP的A组光镜照片显示大鼠肝细胞内外均未见特异性标记银粒显影,而灌流液中含37 MBq[α-32P]ATP的B组光镜照片显示大鼠肝细胞内可见多个大小不等的[α-32P]ATP自显影银粒分布,而肝窦及肝小叶中央静脉等血管内则几乎无黑色自显影银粒分布。

Finally confirmed that,The thighbone and the osteoporosis morbidity is possibly connected protein 6, respectively are: The lactoferrin light chain, membrane association protein A3, the enolase, ATP gather the enzyme, the acetyl coenzyme A reductases, the myo calcium protein; The lumbar vertebra and the osteoporosis morbidity is possibly connected protein 5, respectively are: The actin, the keratin, the enolase, ATP gather the enzyme, the myosin; The thighbone and the strong bone valuable curative effect is possibly connected protein 9, respectively are: The enolase, ATP gather the enzyme, the myo-calcium protein, the creatine activating enzyme isozyme, the phosphoglyceric acid change flavor the enzyme, the myosin, the lactoferrin light chain, the pyruvic acid activating enzyme isozyme, the crown protein; The lumbar vertebra and the strong bone valuable curative effect are possibly connected protein 8, respectively are: The carbonic anhydrase, the actin, the αB-crystal protein, 3-phospho-glycerol aldehyde oxidase, the serum albumin, ATP gather the enzyme, the myosin, the enolase.

最后确认:股骨与骨质疏松发病可能相关的蛋白6个,分别为:乳铁蛋白轻链、膜联蛋白A3、烯醇化酶、ATP合酶、乙酰辅酶A还原酶、肌钙蛋白;腰椎与骨质疏松发病可能相关的蛋白5个,分别为:肌动蛋白、角蛋白、烯醇化酶、ATP合酶、肌球蛋白;股骨与强骨宝疗效可能相关的蛋白9个,分别为:烯醇化酶、ATP合酶、肌钙蛋白、肌酸激酶同工酶、磷酸甘油酸变味酶、肌球蛋白、乳铁蛋白轻链、丙酮酸激酶同工酶、冠蛋白;腰椎与强骨宝疗效可能相关的蛋白8个,分别为:碳酸酐酶、肌动蛋白、αB-晶体蛋白、3-磷酸甘油醛脱氢酶、血清白蛋白、ATP合酶、肌球蛋白、烯醇化酶。

ATP activated current was potentiated markedly by preapplication of BK.The enhancement of BK was depndent on the concentration of BK and ATP.

预加BK30S后再加ATP,则ATP激活电流明显增强,其电流幅值的增强作用依赖于BK及ATP浓度。

Methods: Eleven B-CLL patients were studied. Leukemic lymphocytes with (n=8) or without (n=3) P2z receptors were exposed in vitro to ATP, benzoylbenzoic-ATP, 2-methylthio-ATP(2MeSATP), adenosine-5′-[γ-thio] triphosphate, and other nucleosides for 8h. Apoptosis was detected by electron microscopy, agarose gel electrophoresis, and quantitative TdT assay. Results:Apoptosis was detected only in leukemic lymphocytes with P2z receptors. By using the quantitative assay, ATP-inducing DNA strand breaks were found to occur specifically for BzATP, ATP and 2MeSATP, but not for ATP-γS and other nucleosides.

将表达P2z受体[P2z]与不含P2z受体[P2z]的两组CLL细胞分别同1.0mmol/L三磷酸腺苷体外培养8小时,以电镜、DNA凝胶电泳和定量DNA 3′端TdT法检测细胞凋亡;并对ATP、苯甲酰苯甲酸ATP、2-甲基硫ATP(2MeSATP)、γ-硫代ATP及其它核苷的诱导效应和氧化型ATP、1-[N,O-二(5-异喹啉碘酰基)N-甲基-L-酪氨酰]-4-苯哌嗪KN-62)的抑制效应做定量研究。

These results suggested that in chloroplast ATP synthase, both the N-terminus and C-terminus of the ε subunit show importance in regulation of the ATPase activity. Furthermore, the N-terminus of the ε subunit is more important for its interaction with γ and some CF〓 subunits, and crucial for the blocking of proton leakage. Compared with the ε subunit from E. coli, the chloroplast ε subunit is more sensible to N-terminal or Cterminal truncations.

从这些实验结果中可以看出:(1)叶绿体ATP合酶ε-亚基的N端和C端对于其功能的发挥都很重要;(2)ε亚基N端和C端氨基酸在抑制ATP水解和堵塞质子泄漏两个功能上起着不同的作用;(3)与细菌ATP合酶相比,叶绿体ATP合酶ε亚基N端和C端的缺失对其功能的影响更为显著。

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Knee Deep At ATP
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I didn't watch TV last night, because it .

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Since this year, in a lot of villages of Beijing, TV of elevator liquid crystal was removed.

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