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The method comprises the following steps: according to the raw water quality, the change of the number of bacteria inside the sedimentation tank and the water quality of the backflush yielding water, the backflush yielding water in the sedimentation tank is collected and deposited in a backflush phase of a working period; supernatant fluid containing mass active bacteria and soluble nutrient elements reflow to the sedimentation tank; total or partial sediment containing soluble nutrient elements in an underlayer reflow to the sedimentation tank and is reutilized by mass microorganisms in the sedimentation tank, thereby replenishing the nutrient substrate needed for microorganism growth, proliferation and metabolism under the condition of the low nutrition substrate, and maintaining the ecological stability in the sedimentation tank.

该方法根据原水水质和生物滤池内部细菌数量的变化以及反冲洗出水的水质,将生物滤池工作周期中反冲洗阶段的反冲洗出水收集并沉淀,将其含有大量活性细菌和溶解性营养元素的上清液回流至生物滤池,下层含有不溶性营养物质的沉淀全部或部分回流至生物滤池,被生物滤池当中的大量存在的微生物重新利用,从而补充在低营养基质条件下,微生物生长、增殖和新陈代谢所必需的营养基质,维持生物滤池当中的生态稳定。

The strain JCR5 can grow on many substrates other than EE2 such as several steroid estrogens (estrone, 17β-estradiol, estriol and mestranol), intermediate chemicals in contraceptive medicine processing and some aroma chemicals.

葡萄糖、17β-雌二醇(E2)分别与EE2的共基质代谢试验表明,在共基质条件下,葡萄糖的存在对EE2的降解起到一定的促进作用,而E2的存在对EE2的降解具有一定的抑制作用。

Objective: The purpose of our studies are gaining a better insight into the effect of genistein on mesangial cell"s phenotype change and ECM expression plus degradation under DN circumstances.We add genistein with different concentrations in high glucose cultured rat mesangial cells;feed DM rats with the single concentration genistein for different days;to explore the expression of SMemb,the mark of mesangial cell"s hypertrophy phenotype change;to examine the synthesis of Fn as well as the change of the balance between MMP-2 and TIMP-l;to comprehend its effect on renal pathological changes of DM rats and some related factors;trying toexplore the possible mechanisms.Through these studies,we will have some information about the experimental value of genistein in DN field.

目的:为了研究金雀异黄素对DN环境下大鼠MC肥大表型转换标志物SMemb和ECM分泌及降解的影响,我们拟在细胞水平以不同浓度的金雀异黄素作用于高糖培养下大鼠MC,在动物水平以同一浓度的金雀异黄素作用于DM大鼠不同时间,观察细胞表型转换标志物SMemb、ECM主要成分Fn、ECM降解酶系统基质金属蛋白酶—2(MMP-2)/基质金属蛋白酶抑制剂—1(TIMP-1)表达的变化,同时观察金雀异黄素对DM大鼠肾脏病理及影响肾脏病进展的糖脂代谢紊乱的影响,并进一步探讨金雀异黄素发挥作用的可能机制;为明确金雀异黄素在DN治疗中的地位及意义提供实验依据。

The results show that the compound conductive fiber has typical structure of sheath-core consists of black greened polyaniline electric conductive deposition as the skin and the white polypropylene matrix fiber as the core, which makes the compound fiber preferable physical mechanical property. The intensity and the elongation ratio of the electric conductive fiber are decreased but the thermal stability is enhanced after modified. The compound fiber has the good acid resistance but poor base resistance. The thermal stability of the compound fiber prepared by 4-methyl-benzene sulfonic acid is better than that prepared by hydrochloride acid. Moreover, the compound fiber can be re-doped by other organic or inorganic acid after freed from the adsorbed acid. Furthermore, the electric conductivity of the compound fiber decreases with the temperature increasing but hardly changed with the humidity. The adsorptive ability and therefore the content of the polyaniline, the constant of electric conduction, and the durability of the compound fiber can be enhanced by thinning the diameter, section heteromorphosis, section heteromorphosis and plasma treatment of the surface or blending with COPET of the fiber.

结果表明:复合纤维是聚丙烯与聚苯胺的共混体系,具有典型的皮芯型结构,皮层为墨绿色的聚苯胺沉积层,形成连续的导电通道,芯层为白色的聚丙烯基质纤维,提供物理机械性能;导电改性后纤维的强度、强力和伸长率均有下降,但热稳定性得到提高;复合纤维的耐酸性比耐碱性好,以对甲苯磺酸做掺杂酸比盐酸掺杂聚苯胺热稳定性好,脱掺杂后的复合纤维,可用其它无机酸或有机酸进行再掺杂;复合导电纤维的电导率随温度升高降低幅度较大,但几乎不受湿度影响;基质纤维细旦化、截面异形化、表面等离子体处理或共混COPET等改性处理均能提高纤维的吸附性,进而提高复合纤维表面聚苯胺含量、电导率和耐久性。

All enhancers did not significantly change the transcorneal lag time of ENX. The irritancy of poloxamer and Azone was observed.? The results of in vitro release studies showed that the ENX gel based 3% HPMC K4M and 3%HPMC F4M povided sustained release of the drug over an 8-h period in vitro.Diffusion area has significantly effect on drug release, and pH value of medium and rotation rate have effcet on drug release.However, the diffusion shield has no effect on drug release. The P_ value of the preparation based on 3% HPMC F4M was 1.34-fold of conventional eye drops of ENX.

体外溶出度试验结果表明,以3%的HPMC K4M和F4M为基质制备的ENX凝胶剂的体外释放行为符合眼用缓释制剂的要求;体外释放度影响因素试验结果表明,释放面积对释放度有显著性影响,pH值和转速略有影响,而扩散屏障没有影响;离体角膜透过实验结果表明,以F4M为基质制备的凝胶剂中ENX的表观渗透系数P_(app是对照组的1.34倍,说明F4M与眼角膜的相容性较好,是一种理想的眼用制剂增稠剂,可以在眼用制剂中广泛采用。

Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有按摩明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数按摩明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

Methods Cell culture,flow cytometry,HE staining,Nigrosine staining and electron microscopy were used. Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

The results show that:①The forest soils have the stronger nitrification, but also the nitrification in surface horizon is stronger than the undersoil's.

结果表明:①森林土壤有较强的硝化活性,且表土层比底层土强,同时根际土利于硝化作用进行,根际效应R/S在4.5左右;②淹水厌气培养24h,-N的消失率为52%~58%,占第10天的55%~71%,且表土层-N的消失率比底层土大;③参与同化反硝化作用的还原酶活性较强,在培养24h后,被还原的基质数量占加入基质数量的70%~90%。

But Lovelock saw that if you had a vast network of coevolutionary impulses, such that no creatures could escape creating its own substrate and the substrate its own creatures, then the web of coevolution spread around until it closed a circuit of self-making and self-control.

但洛夫洛克别有见地,他认为,假使有一张具有共同进化冲劲的大网,它网罗所有生物使其无可逃遁,生物创造自身存活所在的基质,而基质又创造存活其中的生物,这个共同进化的网络就会向周围扩展直到封闭成为一个自给自足、自我控制的轮回。

At the same time, the rhizosphere is favourable to the nitrification, the rhizosphere effect R/S is about 4.5;②The loss rate of -N in 24 h in flooded and anaerobic incubation is 52%?

58%,占第10天的55%?71%,且表土层-N的消失率比底层土大;③参与同化反硝化作用的还原酶活性较强,在培养24h后,被还原的基质数量占加入基质数量的70%?

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Breath, muscle contraction of the buttocks; arch body, as far as possible to hold his head, right leg straight towards the ceiling (peg-leg knee in order to avoid muscle tension).

呼气,收缩臀部肌肉;拱起身体,尽量抬起头来,右腿伸直朝向天花板(膝微屈,以避免肌肉紧张)。

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However, to get a true quote, you will need to provide detailed personal and financial information.

然而,要让一个真正的引用,你需要提供详细的个人和财务信息。