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Level of fasting blood sugar, total protein, albumin, alkaline phosphatase and potassium significantly increased, respectively.

快速血糖水平,总蛋白,白蛋白,碱性磷酸酶和钾的水平都有相应的显著上升。

For nearly thirty years the reactions of protein phosphorylation-dephosphorylation involving protein kinases and phosphoprotein phosphatases have been recognized as means of reversibly modulating the function of proteins.

数十年的研究表明,由蛋白激酶和蛋白磷酸酶催化的蛋白质磷酸化-去磷酸化反应是可逆地调节蛋白质功能的重要方式。

Retinogenesis; photoreceptors; visual pigments; color vision; photoreception; phototransduction; visual purple; opsin; rhodopsin; retina; 11-cis-retinal; vitamin A; chromophores; fovea centralis; macula lutea; recoverin; guanylate cyclase

retinogenesis;光感受器;视色素;色视觉;光感受;光传导;视紫红质;视蛋白;视紫质;视网膜;11 - cis -视网膜的;抗干眼醇;发色团;中央凹;黄斑;恢复蛋白;鸟苷酸环化酶首页上一页共有 15 条记录,本页从第 11 到第 15 条。

Pokeweed antiviral protein, a 29-kD protein isolated from Phytolacca americana, inhibits translation by catalytically removing a specific adenine residue from the large rRNA of the 60s subunit of eukaryotic ribosomes. In addition to its ribosome-inactivating ability, PAP has potent antiviral activity against many plants and animal viruses.

美洲商陆抗病毒蛋白(pokeweed antiviral proteins,PAPs),是在美洲商陆的不同组织或不同生长阶段生成的一类具酶功能的单链核糖体失活蛋白(ribosome-inactivating proteins,RIP),是天然的广谱抗病毒生物活性物资,能抗多种植物和动物病毒。

Methods Blood samples were collected from the precaval vein of 6 female Tibet mini-pigs to test the concentration of sex hormones including T,P4,E2,FSH,LH,PRL and blood biochemical indexes including Ca, Mg, P, ALP, Cre, CHO, TP, and Alb during the estrous cycle.

对6头雌性西藏小型猪在发情周期内的发情当天、第5天、第10天、第15天、再次发情时分别采血5 mL并分离血清,应用放射免疫法测定血清睾酮、孕酮(P4)、雌二醇(E2)、促卵泡生成激素、促黄体生成激素、泌乳素;用自动生化仪测定血清钙、镁、磷、碱性磷酸酶、肌苷、总胆固醇、总蛋白、白蛋白。

Usually they exist as proenzyme, but after activation, they rapidly attack the blood brain barrier, degrade some matrix proteins of the basis membrane, break down the endothelial cell close connection protein, and promote the hydro-cephalus formation and phlogocyte infiltrating.

通常它们以酶原的形式存在,一旦活化,则迅速攻击血脑屏障,降解基底膜的一些基质蛋白,破坏内皮细胞的紧密连接蛋白,促进脑水肿的形成和炎细胞的浸润。

The in vivo competitive binding test was study by adding the segment protein which CREG most binding to into the supernatant with wt/mCREG receptively. The change of CREG biologic effects on VSMC were analyseses to identified the direct binding of CREG to IGF2R domains.

将与wt/mCREG蛋白高亲合的M6P/IGF2R胞外重组小肽片段分别添加到细胞培养上清中,确定wt/mCREG蛋白对VSMC生物学行为的调控作用(流式细胞分析检测细胞增殖、刮伤实验和明胶酶谱分析细胞迁移能力)是否通过其与M6P/IGF2R小肽的直接亲合作用介导。

Methods Forty women and their babies (40) were enrolled in this study. Placental tissues were assayed for leptin mRNA by reverse transcription/polymerase chain reaction, and assayed for the obese gene protein leptin by Western-blot and immunohistochemistry. Blood was taken from the umbilical cord of the babies at delivery. Serum leptin was measured by radio-immunoassay. Neonatal anthropometric measurements were recorded within 48 hours after delivery.

方法在40例产妇分娩时采集胎盘与脐血,采用逆转录聚合酶链反应检测胎盘肥胖基因mRNA相对表达水平,采用Western-Blot检测胎盘肥胖基因蛋白表达水平,采用免疫组化观察胎盘肥胖基因蛋白表达位点,采用放射免疫法检测脐血瘦素水平,采用Ponderal指数[PI=100×体重/身长3]估测新生儿营养状态。

In this thesis, ribonuclease A was employed as a model protein to understand the formation of correct three-dimensional structure in the refolding of recombinant proteins in vitro. On this basis, the refolding mechanism in vitro was discussed.

本文以核糖核酸酶A为蛋白质体外重折叠的模型蛋白,对其体外重折叠过程进行了研究,探讨了这类目标蛋白复性过程的一些规律性的问题。

And Homo Sapien fetal brain cDNA Library was used to screen PRL-3-interacting proteins. 3. Identification and bioinformatical analysis of CDH22, a candidate PRL-3-interacting protein Interaction between PRL-3 and CDH22, a candidate PRL-3- interacting protein was identified by GST-pull down assay, co-immunoprecipitation assay and co-localization analysis in vivo and in vitro.

PRL-3相互作用蛋白的鉴定及其功能的生物信息学分析运用基于蛋白质水平的谷胱甘肽-S-转移酶融合蛋白沉淀、免疫共沉淀和共定位分析等技术对酵母双杂交系统初步筛选的结果进行体内和体外的验证。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。