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vitro相关的网络例句

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与 vitro 相关的网络例句 [注:此内容来源于网络,仅供参考]

In the present study we transfected F-GFP into cultured hippocampal neurons at 5 days in vitro(DIV 5).Then ASICs antagonists were applied to the neuronal medium to inhibit the function of ASICs.Dendritic growth and arborization of cultured hippoeampal neuron were observed in DIV8 and DIV14. We attempted to determine whether and how ASICs regulate dendritic development.

在本研究中,我们在体外培养第五天(days in vitro,DIV5)的原代海马神经元中转染定位在膜上的GFP,随后加入ASICs拮抗剂抑制ASICs的功能,观察DIV8和DIV14这两个时间点海马神经元的树突生长、分支复杂程度,来研究酸敏感离子通道是否会影响海马神经元的树突发育。

The discussion of the degradation mechanism: Chitosan is not hydrolyze in neutral soak in vitro. The mechanism of degradation of the PDLLA membrane in vivo and in vitro is similar, both represent the simple hydrolyze. The degradation of he composite membrane mainly represent the PDLLA hydrolyze of, chitosan can hydrolyze when there are acid product which is PDLLA's catabolite in vitro.

降解机理探讨:壳聚糖膜体外中性条件下不水解;聚乳酸膜体内外降解机理相似,都表现为简单水解机理;复合膜体外降解主要表现为聚乳酸的水解,壳聚糖在聚乳酸降解后产生酸性产物的条件下存在酸水解机理。

Techniques in embryo technology (such as in vitro production of embryos and animal cloning) need large quantities of high quality oocytes. But the quality of in vitro matured oocytes from slaughtered animals is generally lower than that of the in vivo matured oocytes. It is usually thought that the reason for this poor quality in in vitro matured oocytes is the lack of capacitation during the dominancy of follicular development in vivo.

目前胚胎工程技术研究和开发(如体外生产胚胎和体细胞克隆等)需要大量高质量的成熟卵母细胞,但利用屠宰动物卵巢卵母细胞经过体外成熟培养而获取的卵母细胞质量还远不如体内成熟卵母细胞,其原因一般认为是由于缺乏体内主卵泡阶段的获能作用。

This process aims at recapitulating the normal embryologic development of the organ of interest. The main difference between in vivo technology and in vitro technology is: in vitro technology emphasis on in vitro cell culture. It has special value for the specific tissue such as articular cartilage.

体内组织工程技术与体外组织工程技术的目标相同,都是实现组织完全再生;区别在于其达到再生的方法:体外组织工程技术强调细胞的体外培养,并使这些细胞产生功能,这对有些组织有特殊价值,如软骨。

The results shown as follow: 1. The study on mice denuded oocytesin vitro maturation, in vitro fertilizationand in vitro development. This part of paper is to discuss whether the remove of granulose cells can affect the mice oocytes maturation rates, fertilization rates and development rates in vitro.

一、去除卵丘细胞的小鼠卵母细胞的体外成熟、体外受精初步研究本实验探讨了不同成分明确的成熟培养液对去除卵丘细胞的小鼠卵母细胞的体外成熟、体外受精和胚胎的体外发育的影响。

Using TaKaRa LA PCR? in vitro Clonging Kit, a 2.3kb DNA fragment from the mutant was amplified and identified. Sequence analysis indicated that the fragment was composed of a complete proE gene and a partial proA gene.

根据枯草芽孢杆菌93151野生菌株proB基因的序列设计并合成引物,利用TaKaRa LA PCR~ in vitro Clonging Kit试剂盒,克隆突变菌株的proBA基因,得到一个约2.3kb的DNA片段,序列分析表明该片段包含一个完整的proB基因和不完整的proA基因。

The data collected from in vitro and in sacco digestive trials showed that suplementing BYC can significantly increate fiber digestibility.

In sacco及In vitro的消化试验均表明,BYC对饲料粗纤维素的消化率均有极显著的(p.01)促进作用。

Proliferating satellite cells express acidic fibroblast growth factor during in vitro myogenesis.

在在vitro myogenesis期间增生的人造卫星房间表达酸性的纤维原细胞生长因素。

This experiment first studied in the mature nutrient medium to increase the hormone to the porine ovocyte in vitro mature process in the chromosome configuration and the mature rate influence, by explored the porine ovocyte in vitro mature rule, enhanced in vitro raise maturity, was the ROSI technology system preparation high quality ovocyte; Then has carried on the experiment in view of the porine round sperm cell in vitro separation, through to the ROSI operation and ICSI (Intracytoplasmic sperm injection, the comparison which ICSI) operated studies has affected the ROSI operation the factor.

本试验首先研究了成熟培养液中添加激素对猪卵母细胞体外成熟过程中染色体构型和成熟率的影响,以探索猪卵母细胞体外成熟规律,提高体外培养成熟度,为ROSI技术体系准备优质卵母细胞;然后针对猪圆形精细胞的体外分离进行了试验,进而通过对ROSI操作和ICSI(Intracytoplasmic sperm injection,ICSI)操作的比较研究了影响ROSI操作的因素。

Furthermore there are more apoptosis cells in inner root sheath than in outer root sheath. Conclusion When we culture human hair follicle in vitro, Williams E serum-free medium is a suitable choice.This model is a fine model also, which is used for screening drug that may accelerate or inhibit the hair growth.Cryo-section can simplify procedure of paraffin section in histology detection of culture human hair follicle in vitro.We can observe the ultrastructural change of human hair follicle in vitro by transmission electron microscope,which can assist to observe apoptosis cells. The eyepiece micrometer is a simple tool for measuring length of hair follicle in vitro.

在离体培养人头皮毛囊时,Williams E无血清培养基是合适的选择,该模型也是筛选促进或抑制毛发生长药物的良好模型;离体培养毛囊组织学检测用冰冻切片可以简化步骤;透射电镜可以用来观察离体培养的毛囊的形态和超微结构的变化,也可以用来协助观察细胞凋亡的状况。

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