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2 The result of electron microscope cytochemistry stain: The positive production of ACPase was present black lead phosphate deposit with high electron-dense under light microscope, located in cytoplasm or apophysis mainly. Lysosome was located in cytoplasm in the earlier of differentiation, then was present in apophysis with it grew.

4.2 电镜酶细胞化学染色结果:电镜下ACPase阳性产物为电子致密度高的黑色磷酸铅沉淀,主要分布于神经元的胞浆中或突起内,神经元分化的初期,溶酶体集中分布于胞质内,随突起的长出,可见在突起内出现。

The results showed that 1 there were no significant differences in the rates of cytoplast protrusion and enucleation between oocytes that were incubated in colchicine (0.4 μg/mL) for 0.5 h and oocytes that were incubated in colchicine (0.4 μg/mL) for 1 h, and the rate of cytoplast protusion can be 85.4% while the rate of cytoplast enucleation is 100%. 2 There was no significant difference in oocyte enucleation between oocytes treated with medium containing 0.2 μg/mL colchicine for 0.5 h and oocytes treated with medium containing 0.4 μg/mL colchicine for 0.5 h. 3 A maturation time of 18–23 h did not affect the rates of cytoplast protusion and enucleation by chemically assisted enucleation, whereas the rate of enucleation of oocytes by blind enucleation was found to decrease with a prolonged incubation time. 4 The development rates of reconstructed embryos could not be influenced by these two enucleation methods, increased from oocytes matured for 21–23 h.

结果表明: 1 卵母细胞在0.4 mg/mL的秋水仙素溶液中分别孵育0.5 h和1 h,胞质突起率和去核率没有显著的差异,突起率可高达85.4%,去核率达到100%; 2 0.2 mg/mL或0.4 mg/mL秋水仙素溶液将卵母细胞处理0.5 h,对去核效果没有显著影响; 3 对于体外成熟18~23 h的卵母细胞,随着成熟时间的延长,盲吸法的去核率降低,但没有影响秋水仙素诱导胞质突起的比率和去核率; 4 两种去核方法对重构胚的发育没有产生显著影响,但成熟21~23 h卵母细胞重构胚囊胚的发育率显著高于成熟18~20 h卵母细胞重构胚囊胚的发育率。

Any of the minute hairlike structures projecting from the surface of certain types of ''.

微绒毛;微小突起物;指状突起一些上皮细胞表面上突起的微小发状结构的总称,尤指小肠上的

Figure 17.2 Distribution of papillae along the dorsal surface of the tongue: C, circumvallate; Fu, fungiform; Fi, filiform.

图17.2 顺着舌头表面的乳状突起的示意图: C,壁垒状突起;Fu,菌状突起;Fi,覆叶状突起。

A knoblike protuberance arising from a surface, as the prominence near the hinge of a bivalve shell or the projection at the scale tip of a seed-bearing cone.

圆形隆起在一个表面突起的圆形装饰物似的隆起,如在双壳贝类贝壳边缘附近的突起或在含种子的球果顶端的突起

A knoblike protuberance arising from a surface, as the prom nce near the hinge of a bivalve shell or the projection at the scale tip of a seed - bearing cone.

圆形 隆起在一个表面突起的圆形装饰物似的隆起,如在双壳贝类贝壳边缘附近的突起或在含种子的球果顶端的突起

The results indicate that: the macroslructural features of seed surface, including smooth type, rugulose type and tuberculate type, may suggest the evolutionary trend from smooth type to rugulose type, from rugulose type to tuberculate type; the microstructural features of outer epidermis can be divided into two types, viz. verrucate type and reticulate type. The former included S. grandiflora, S. chinensis, S. elongata, S. lancifolia, S pubescens, S. henryi, S. repanda, the latter included S. propinqua and .S. plena.

结果表明:该属的种子宏观形态呈现平滑、细皱纹或瘤状突起,并认为五味子属种子形态可能有从平滑到有细皱纹再到有瘤状突起的演化趋势;该属种皮表面微观形态可分为疣状突起型(如:大花五味子、北五味子、东亚五味子、狭叶五味子、毛叶五味子、翼梗五味子和二色五味子)和网纹型。

These towers differentiate and form small bulb by two ways: one way is that towers begin to differentiate from their center ; another is that towers begin to differentiate from the tops of towers or their sides and appear small sunken concaves.

这些突起进一步分化为小鳞茎是通过两种分化方式:一种是先从突起中央出现分生细胞团开始分化的;一种是先从突起的顶端或一侧出现小凹沟开始分化的。

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。

GnRH 1R neurons were found as early as on the first day of culture. During the 1st-3rd days in vitro, they grew fastest. The average growth rates of the perikarya and processes were 45 59μm 2/d and 19 39μm/d, respectively.

培养1d即可见GnRH-IR神经元;1~3d,GnRH-IR神经元生长最快,胞体和突起的平均生长速度分别为45.59μm2/d和19.39μm/d,染色加深;培养7d,GnRH-IR神经元的胞体截面积、胞体染色强度和突起长度均达最高峰,分别为171.21±43.17μm2,0.289±0.034,87.01±22.33μm;培养14d,GnRH-IR神经元的胞体大小和突起长度维持在7d时的水平,但染色减弱。

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They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.

他们没有侵略性,但我大喊,并在他们的方向扔石头让他们过的线索,远离我,以防万一。

In slot 2 in your bag put wrapping paper, quantity does not matter in this case.

在你的书包里槽2把包装纸、数量无关紧要。

Store this product in a sealed, lightproof, dry and cool place.

密封,遮光,置阴凉干燥处。