查询词典 ATP

The experimental group corneas were preserved by organ culture for 4 weeks, the corneal thickness was measured with ultrasonic corneal pachymeter. Then every corneas were divided into half -chip, there are 48 half-chip total. It was divided into 4 groups, there are 12 half-chip in every groups. The corneal endothelial cell density of 12 half-chip were counted through Alizarin Red-Trypan blue staining; 12 half-clip corneas were fixed with 4% neutral formalin solution, HE staining was performed, the expression of AQP-1 in corneal stroma and corneal endothelial cell were detected through immunohistochemical staining; Na~+-K~+-ATPase activities in 12 half-clip corneas were examined with Na~+-K~+-ATPase kit; the expression of AQP-1 mRNA were detected through real-time fluorescent quantitation PCR.

实验组经器官培养保存4周后以角膜测厚仪测量角膜厚度，然后每个角膜被分成两半，共48个半片角膜，再分成4组，每组12个半片。12个半片用茜素红-台盼蓝染色染色行角膜内皮细胞计数；12个半片角膜用4%中性福尔马林溶液固定行HE染色、应用免疫组化染色检测AQP-1在角膜基质和内皮细胞表达的改变；12个半片角膜用Na~+-K~+-ATP酶试剂盒测量角膜内皮细胞Na~+-K~+-ATP酶活性；12个半片角膜用实时荧光定量PCR检测AQP-1mRNA表达改变。

The general situations of the eye were observed and the corneal thickness were measured with ultrasonic corneal pachymeter after the animal models was established. After a week, the corneas were removed after the experimental animals are put to death. The corneal endothelial cell density of 12 half-chip were counted through Alizarin Red-Trypan blue staining; 12 half-clip corneas were fixed with 4% neutral formalin solution , HE staining was performed, the expression of AQP-1 in corneal stroma and corneal endothelial cell were detected through immunohistochemical staining; Na~+-K~+-ATPase activities in 12 half-clip corneas were examined with Na~+-K~+-ATPase kit; the expression of AQP-1 mRNA were detected through real-time fluorescent quantitation PCR.

术后观察眼球大体情况、测量角膜厚度。1周后处死实验动物取角膜，用茜素红-台盼蓝染色染色行角膜内皮细胞计数；用4%中性福尔马林溶液固定行HE染色、应用免疫组化染色检测AQP-1在角膜基质和内皮细胞表达的改变；用Na~+-K~+-ATP酶试剂盒测量角膜内皮细胞Na~+-K~+-ATP酶活性；实时荧光定量PCR检测AQP-1mRNA在角膜内皮细胞表达的改变；并于正常对照组角膜比较。

Results: The concentration of intracellular plasmic free calcium was lower in irradiated group than in control group (P. 05), and the activity of plasma membrane Ca2+-Mg2+-ATPase increased significantly.

结果：照射后淋巴细胞内游离钙浓度明显低于正常(P＜0.05)；同时细胞膜Ca2+-Mg2+-ATP酶活性增加(P＜0.05)；而且照射后细胞内游离钙浓度降低与质膜上Ca2+-Mg2+-ATP酶的激活呈负相关。

And then he was in full control, outplaying, out smarting and out hitting the clay court specialist to capture the inaugural Shanghai Masters 1000 dismissing world No.

接下来他完全控制了比赛，无论是在球技、心理素质还是力度上都彻底地压倒了&红土专家&，以7-6(3)和6-3的比分击败排名第2的Rafael Nadal，登上了上海ATP 1000大师的宝座，为他取得参加伦敦巴克莱ATP世界巡回赛决赛的资格奠定了坚实基础。

The results indicate that both the on/off of release of ATP and the amount of released ATP can be controlled by applying appropriate potential on the electrode.

通过控制不同的电位可以控制释放的时间及释放量的多少。这种电极在研究神经组织的活动和改变传统的给药方式方面有很重要的意义。

When those enzymes are activated by AMPK, they would shut down the energy-consuming biosynthesis pathway and turn on the energy-producing fatty acid oxidation pathway.

他们的活性受到抑制后，能够关闭消耗大量ATP的生物合成代谢途径而打开产生大量ATP的生物分解代谢途径。

The electron transfer chain system locates in the inner membrane of mitochondria and is made up of four large trans-membrane protein complexs, ubiquinone and cytochrome c, which is coupled with Complex V, forming the mitochondrial oxidation-phosphorylation system, producing most of the energy.

呼吸链的功能是进行生物氧化，并与称之为复合物 V 的 ATP 酶偶联，共同完成氧化磷酸化制造生物能量分子 ATP 的功能。

No immunostaining was seen in RPE. Double staining that Kir2. 1 and glutamine synthetase, Kir2. 1 and glutamine synthetase colocalized well. Intense Kir7. 1 immunolabeling was present on the apical surface of all RPE cells and appeared to extend over the length of the apical processes. Na〓, K〓-ATPase expression varied among RPE cells, but in highly expressing cells, it co-localized with Kir7. 1. Immunoreactivity of Kir2. 1、Kir4. 1 and Kir7. 1 acomplished by ABC immunohistochemistry in monkey and human retinae got the nearly same results as bovine.

间接免疫荧光组织化学显示，Kir2.1蛋白主要分布在Müller细胞与神经元相接触的细胞膜区域；与Müller细胞的特异性标记蛋白质抗谷氨酸合成酶抗体双重标记显示其分布特性重叠，在RPE未检测Kir2.1蛋白的免疫活性存在；Kir4.1蛋白集中分布于Müller细胞的内侧突起，与GS蛋白双重标记显示其分布特性重叠，RPE未检测Kir4.1蛋白的免疫活性存在；Kir7.1主要分布于RPE游离面及其突起的全长，与特异性标记RPE突起的Ezrin蛋白完全重叠，Na〓-K〓ATP酶在不同部位的RPE表达不同，Na〓-K〓ATP高表达的RPE细胞与Kir7.1的分布特性重叠。

Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA

来自北卡罗来那大学医学院的研究人员发现凋亡细胞释放ATP和UTP，它们对表达P2Y2 ATP/UTP受体的吞噬细胞来说充当一种&找到我&信号及化学引诱剂。

Results: Carbonic anhydrase, Na+-K+-AT -Pase, Mg2+--ATPase, 5'-nucleotidase and NADPH oxidase could manifest enzyme activity on endosome membrane in the renal proximal tubules、hepatic cell of rat and human leukocytes.

结果 上述碳酸酐酶，Mg2+-ATP酶，Na+-K+-ATP酶，5'-核苷酸酶及NADPH oxidase分别在大鼠肾脏近曲小管，肝脏及人体白细胞的内吞体膜上都有酶活性存在。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。