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protein相关的网络例句

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与 protein 相关的网络例句 [注:此内容来源于网络,仅供参考]

Rickettsii. The purified 120kDa protein and P5 protein were recognized by sera from animals infected with agents of the genus rickettsia, not Coxiella burnetii and Orientia tsutsugamushi., suggesting the two antigens are specific for genus rickettsia.

120kDa蛋白和P5蛋白可与立克次体属的多种立克次体免疫血清发生交叉反应,与贝氏柯克斯体、恙虫病东方体不反应,提示这两种蛋白具有立克次体属特异性。

RNA interference, which specifically inhibits protein expression, is a new approach to the study of protein function.

RNA干扰技术能够高效、特异的抑制目的蛋白的表达,因此是一种有利的蛋白功能研究技术。

Over the years, Rosetta has evolved to also include protein design and the prediction of protein complexes.

经过多年的发展,Rosetta 已经具备了蛋白质设计及蛋白质聚合物预测的能力。

Ingredient: High Concentrating Silk Protein, Hyaluronic Acid, Roxburgh Rose Extract, Vitamin E, Micro-collagen Protein

高浓缩蚕丝蛋白、透明质酸、刺梨提取液、 VE 、小分子胶原蛋白。

The main objective is to conserve the digestible fiber, protein, and energy in the forage, and to maintain the protein in a form that can be utilized efficiently by the ruminant animal.

青贮加工的主要目的就是保存牧草中的可消化纤维、蛋白质及能量,将蛋白质保持为反刍动物能够有效地利用的一种形式。

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。

This product union and the optimal near ten years for the domestic feed enterprise, the cultivation factory design's cattle and sheep feed formula, strengthened Va, Vd, Ve, the nicotine acid and the biological element specially and so on, and have included the rumen protein, the rich electrolyte, the trace element, the chelating agent, the seasoner, metabolism regulation medicinal preparation, the nutrition comprehensive and are balanced, may adjust the meat cattle and sheep microcycle, maximum limit enhance the meat cattle's and sheep's protein and do the material amount of radiation, display its heredity potential fully, enhance the cattle and sheep to increase the heavy speed.

本产品结合和优选近十年为国内饲料企业、养殖厂设计的牛羊饲料配方,特别强化了 Va 、 Vd 、 Ve 、烟酸和生物素等,并含有过瘤胃蛋白质、丰富电解质、微量元素、螯合剂、调味剂、代谢调控剂,营养全面且平衡,可调节肉牛羊微循环,最大限度的提高肉牛羊的蛋白质及干物质摄入量,充分发挥其遗传潜力,提高牛羊增重速度。

The difference between codon choice randomization in the region of protein regular secondary structure and that in coil region is investigated in detail. We find that the folding free energy of mRNA segments in different protein secondary structures is significantly different. The average Z score is -1. 38 and -1. 71 for regular secondary structure, but -0.93 and -1. 03 for coil.

我们仔细分析了在蛋白质规则结构区域(alpha螺旋和beta折叠)和无规则结构区域密码子随机选择的差异,发现处于不同蛋白质二级结构的mRNA片段的折叠自由能有显著的不同,对于规则结构,Human和E.coli的平均Z-score值分别为-1.71和-1.38,但是无规则结构的Z-score值分别为-1.03和-0.93。

Aureus secretor strain in a media containing vegetarian amino acids or peptides instead of animal peptides, harvesting the Protein A-containing media and purifying the Protein A by applying it to a synthetic resin that lacks animal peptides and filtering the elutant from the resin.

本发明涉及制备没有动物源产物污染的蛋白A的方法,其包括通过在含有植物氨基酸或肽代替动物肽的培养基中发酵金黄色葡萄球菌分泌菌株,收集含有蛋白A的培养基和纯化蛋白A,并且将其施加到没有动物肽的合成树脂上和过滤来自树脂的洗脱液。

The thesis consists of six chapters. In the first, the technologies of atomic force microscopy and of the measurement elasticity of biomolecules were introduced. In the second, the validity of VSPFM was confirmed by lift mode atomic force microscopy. In this chapter, the height of DNA was measured by lift mode atomic force microscopy, which demonstrated that the method of height measurement of biomolecules by VSPFM was correct and established the foundation of the method of measurement elasticity of biomolecules by vibrating mode scanning polarization force microscopy. In the third chapter, detailed work has been illustrated on the foundation of the method of measurement elasticity of biomolecules by VSPFM. And the compressive elasticity of DNA was measured. In fourth and fifth chapters, the method was applied in the measurement elasticity of proteins. Two proteins elasticity, fibre-like protein α-synuclein and global protein IgG, were measured by VSPFM, through which the method wound its way to the application of biomolecules. In last chapter, the final part of the thesis was a summary. A conclusion of the thesis and a self-comment on my work as a PhD candidate have been made, and expectation about the further works has been addressed.

本论文共分为六章,第一章,引言部分主要介绍了原子力显微镜技术及生物大分子弹性测量技术;第二章主要是VSPFM方法的正确性论证,介绍抬高模式原理,利用抬高模式原子力显微镜对DNA的高度进行测量,论证振动模式扫描极化力显微镜测量生物大分子的高度的正确性以及准确性,从而为振动模式扫描极化力显微镜测量生物大分子的弹性方法的建立奠定基础;第三章以脱氧核糖核酸为例详细介绍了振动模式极化力显微镜测量生物大分子弹性的方法的建立,对DNA的压弹性进行了初步的测量和分析;第四章和第五章介绍了振动模式扫描极化力显微镜在蛋白质弹性测量中的应用:α-synuclein和IgG分别是纤维状蛋白和球状颗粒蛋白,通过振动模式扫描极化力显微镜测量这两种蛋白质的弹性,摸索振动模式扫描极化力显微镜在蛋白质弹性测量中的应用;第六章对全文进行了总结,在对论文的工作进行归纳和自我评价之后,还对进一步的工作进行了展望。

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