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By focusing on the coupling of water and fertilizer and using all-purpose regression design with four factors and five levels, and based on pot experiments and quantitative analysis, the coupling effect of water and fertilizer on Casuarina equsetifolia biomass was studied in order to solve the inconsistency problem of water and fertilizer supply on coastal sandy land.

针对滨海沙地因水肥不协调而形成大面积低效林分的问题,以水肥耦合为中心,以1年生木麻黄幼苗为研究对象,采用四因子五水平二次通用旋转组合设计,利用盆栽试验和定量分析的方法,研究探讨了在不同水肥条件下,水、N、P、K四因子对木麻黄生物量的影响。

Objective After Intense pulsed light irradiation cavia cobaya skin, to evaluate the histological change of skin with HE stains; to evaluate the collagen fiber change with nitroxanthic acid stains; to quantitative analysis of hydroxyproline content. Confirm mechanism of action for Intense pulsed light on sun-damaged human skin.

目的 用强脉冲光照射豚鼠背部皮肤后,通过HE染色观察皮肤组织学的改变;用苦味酸染色观察皮肤胶原纤维的改变;定量分析豚鼠皮肤羟脯氨酸的含量,观察皮肤胶原蛋白的变化,进一步研究强脉冲光治疗皮肤光老化的作用机制。

We localized MMP9 expression in ceil type of the human prostate by using the method of primary cell cultures combined with RT-PCR.

为了深入了解前列腺肿瘤细胞在浸润和转移过程中,与肿瘤侵袭、转移能力相关的异常基因的表达,我们采用单管半定量RT-PCR、酶谱电泳及免疫印迹技术对前列腺癌组织中的MMP-2、MMP-9,TIMP-1、TIMP-2的异常表达情况,在基因及蛋白表达水平上进行了定量分析

An Application of UV and HNO_2 on Selection of Cephalosporium acremonium ;2. The morphologies of Cephalosporium acremonium were quantitatively analysed by bio-image analysis.

利用显微图像分析法对顶头孢霉菌的菌丝形态进行了定量研究,并统计分析了头孢菌素C发酵过程中的菌丝形态的变化规律,具体对菌丝长度、菌丝宽度和菌丝生长单位进行了定量分析,分析了菌丝形态分化与头孢菌素C合成的关系。

This article adopts many methods such as AHP, EFE matrix, IFE matrix and SWOT matrix to analyze the internal and external environment in theory. Combining qualitative analysis with quantitative analysis, this paper provides spare strategy plans that might be adopted by NRHIB. With QSPM matrix this paper analyze the spare schemes and choosable four feasible plans.

在此基础上,本文应用了AHP法、EFE矩阵、IFE矩阵和SWOT矩阵等技术和定量方法,对外部环境和内部环境进行了理论分析,提出了可供企业选择实施的战略方案,利用QSPM矩阵对备选方案进行了定量分析,得出了4个较为可行的战略方案。

Morphometry of numerical density and electron probe X-ray quantitative microanalysis were used to measure the alterations in the number and calcium content of chromaffin granules in adrenal medulla cells during emergency reaction of restrained rats.

采用电镜细胞立体形态计量法及电镜X射线显微定量分析术,对制动应急大鼠的肾上腺髓质细胞内嗜铬颗粒数密度和颗粒内Ca浓度变化进行测量。

The recoveries of seawater and sediment are :naphthalene 73. 0% and 75. 3%, phenanthrene79. 2%and78. 0%, fluoranthene 88. 1% and 80. 7%, pyrene 73. 8% and 70. 2%, chrysene 77. 6% and 72. 8%, benzofluoranthene 87. 6% and 83.6%, benzo pyrene 120. 3% and 110. 0%, respectively.

通过对7种多环芳烃标准样品的高效液相色谱法的定性、定量分析,结果表明,该方法可有效分离PAHs,回收率较高,海水和沉积物中的回收率分别为:萘73.0%和75.3%,菲79.2%和78.0%,荧蒽88.1%和80.7%,芘73.8%和70.2%,屈77.6%和72.8%,苯并荧蒽87.6%和83.6%,苯并芘120.3%和110.0%。

MethodsThe cells of human gastric cancer cell line SGC7901 was treated respectively with Chrysin at different concentration 10、20、40、80μM for 48h. The proliferation inhibitory rate was measured by MTT assay. Acridine orangestaining and flow cytometry were used to detect apoptosis. Western blot assay was used to detect the expression of apoptosis related genes NF拨B,Bcl2,Bax.

方法分别用10、20、40、80μM的ChR处理人胃癌细胞株SGC7901 48h,采用MTT比色法检测ChR对SGC7901细胞的增殖抑制效应;采用丫啶橙染色、流式细胞术检测ChR诱导SGC7901细胞凋亡的发生;应用Westernblot法检测凋亡相关基因NF拨B、Bcl2、Bax的蛋白表达,并用计算机图像分析软件进行半定量分析

Label-free and cleavable isotope-coded affinity tag quantitative proteomic approaches were used to quantify the differential expression of secretory proteins from 3T3-L1 adipocytes with or without insulin stimulation.

首先,采用液相色谱-质谱联用方法对胰岛素刺激与否的3T3-L1脂肪细胞的分泌蛋白进行了大规模的定量分析;胰岛素刺激后,242种分泌蛋白表现为显著变化,其中55种蛋白质下调,187种上调。

Second, this dissertation develops the qualitative and quantitative analysis methods for cogging torque.

其次,本文发展了齿槽力矩的定性和定量分析方法。

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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。