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Methods①The minimum inhibitory concentration and the minimum fungicidal concentration of citral against C.

方法①参照NCCLS M27A方案中的微量液基稀释法测定柠檬醛和氟康唑对原始白念珠菌的最低抑菌浓度和最低杀菌浓度;②采用多步诱导法,观察在含梯度浓度(1~50MIC)柠檬醛培养基上连续转种的白念珠菌MIC的变化情况,以氟康唑作为阳性对照,同时设空白对照和溶媒对照;③将敏感性下降的诱导株在无药培养基上连续转种10次后,检测其MIC值;④测定柠檬醛对氟康唑敏感性下降诱导株的MIC值。

Through determination experiment of AP solutions concentration by using densimeter and thermometer, relation table of temperature-density-concentration of AP solutions was obtained.

通过用密度计和温度计测定高氯酸铵溶液浓度的试验,并由此得到AP溶液的温度-密度-浓度三者之间的关系表,通过该表用密度计和温度计可快速测定AP质量浓度,偏差为±4g/L,符合工艺要求。

According to the characteristic that the isoflavonoids of Derris elliptica Benth have a distinctive absorption spectrum within the ultroviolet wave length range (210 ̄ 345 nm, 290 ̄305 nm), a new method for determining the total isoflavonoids in Derris elliptica Benth by Ultroviolet Spectrometry has been put forward.

根据鱼藤中异黄酮类化合物在紫外光210~245nm及290~305nm处具有吸收峰这一特性,提出了用紫外分光法测定鱼藤中异黄酮类总含量的方法。在300nm波长处,浓度低于6×2.618×10-3/mol·L-1时,测定了标准系列的吸光值,结果表明吸光值与浓度近乎直线相关,相关系数为0.9977;标准系列吸光值准确性高;加样回收率达99%以上;测定样品时,重现性好

61Healthy persons were selected as healthy group. The serum concentration of TGF-β1 was measured by ELISA method; nitre oxide was measured by nitrit reductase method, plasma Ang II was measured by radioimmunoassay.

对高血压病人和61例健康对照者应用酶联免疫吸附法测定血清TGF-β_1浓度,硝酸还原酶法测定NO的浓度,放射免疫分析法测定Ang Ⅱ水平。

The Zetasizer Nano ZS is made in Marvern in England. It is the newest Zetasizer Nano ZS with the newest technology. Malvern Zetasizer Nano ZS90 is for the measurement of size, zeta potential of dispersed particles and the molecular weight of random coiled polymers. If it connect with the Autotitrator, it can measure zeta potential as a function of pH, conductivity or concentration of an additive, provides much greater insight into the processes involved in stabilizing or flocculating disperse systems.

英国马尔文公司生产的Zetasizer Nano ZS型纳米粒度仪是目前世界上技术最先进的纳米粒度仪之一,该仪器可以测定纳米材料的粒度分布、ZETA电位值,并可以进行蛋白质的熔点测定,及蛋白质等大分子和聚合物材料的分子量测试,如果与自动滴定仪相连接后,可自动测定粒度或Zeta电位随pH值、盐浓度或添加剂浓度等的变化趋势。

Based on the absorbance change of indicators with the concentration of hydrogen ion released from the enzyme-catalyzed reaction, a convenient colorimetry method is established for the assay of acidic phospholipase 〓 and glycogen phosphorylase b Brilliant yellow and bromothymol blue are chosen as indicators for assays of acidic phospholipase 〓 and glycogen phosphorylase b by following the absorbance changes at 495 nm and 615nm respectively The method is simple, sample-saving, sensitive and valid for a wide range of enzyme concentrations.

为了研究糖原磷酸化酶的激活动力学和酸性磷脂酶〓的复性过程,我们根据酶催化反应中释放氢离子浓度的变化引起相应的指示剂的光吸收发生变化的原理,建立了一种简捷的比色法,用于测定酸性磷脂酶〓和糖原磷酸化酶b的活性。选用亮黄和溴麝香草酚兰分别作为酸性磷脂酶〓和糖原磷酸化酶b测活的指示剂,在495 nm和615 nm处检测二者的光吸收值的变化,可以测定酶活。本方法的优点是,可在比较宽的酶浓度范围内进行活力测定,而且操作简单、节省样品、灵敏度高。

METHODS: The BEC were preincubated with crocetin (1, 0.1 and 0.01 μmol/L) for 12 h, then exposed to AGE (100 mg/L). The RAGE mRNA expression was detected by RT-PCR analysis, the intercellular adhesion molecule-1(ICAM-1) was measured by ELISA. The extracellular superoxide ion and thiobarbituric acid reactive substances were assessed with superoxide ion kit and colorimetric assay, respectively The intracellular I2O2 was also detected using the probe 2,7-dichlorofluorescein. The mitochondrial membrane potential and mitochondrial Succinate dehydrogenase were analyzed by the retention of rhodamine 123 (Rh123) and MTT.

不同浓度的西红花酸(1、0.1、0.01μmol/L)预孵BEC细胞12h后,用AGE(100mg/L)刺激细胞12h,RT-PCR法测定RAGEmRNA的表达水平;ELISA法测定细胞间黏附分子-(ICAM-1)的表达;试剂盒分别检测胞外超氧阴离子和硫代巴比妥酸反应产物浓度;同时,还用2,7-二氯荧光素测定了胞内H2O2的浓度,并用罗丹明123(Rh123)荧光法及MTT法分别检测细胞线粒体膜电位水平和其琥珀酸脱氢酶的活性。

Dictamnus dasycarps Turcz. also have insecticidal activity to Ostrinia furnacalis, When the concentration was 10g/ml, correct decreased rate reached 92.86%, When the concentration was 0.675ml/g, the correct decreased rate reached 3.57%; Dictamnus dasycarps Turcz. at the range of testing concentration have lower stomach toxic effects to Ostrinia furnacalis.

通过白鲜皮对玉米螟杀虫活性的初步研究表明:白鲜皮对玉米螟表现出很强的拒食活性,在测定浓度范围内其拒食活性均在80%以上,最高可达97.22%。;白鲜皮提取液对玉米螟也有一定的毒杀活性,当浓度为10g/ml时其校正死亡率可达到92.86%,浓度为0.675ml/g时校正死亡率仅为3.57%;白鲜皮在测定浓度范围内对玉米螟的胃毒活性较低,最高才42.86%。

An antibody binding to IGF-IR and inhibiting the binding of IGF-I and IGF-II to IGF-IR which is characterized in that said antibody is a is ofIgG1 isotype, b shows a ratio of IC50 values of inhibition of the binding of IGF-I to IGF-IR to the inhibition of binding of IG-II to IGF-IR of 1:3 to 3:1, c inhibits for at least 80% at a concentration of 5 nM IGF-IR phospohrylation in a cellular phosphorylation assay using 3T3 cells providing 400,000 to 600,000 molecules IGF-IR per cell in a medium containing 0.5% heat inactivated fetal calf serum when compared to such an assay without said antibody, and d shows no IGF-IR stimulating activity measured as IGF-IR phophorylation at a concentration of 10 M in a cellular phosphorylation assay using 3T3 providing 400,000 to 600,000 molecules IGF-IR per cell in a medium containing 0,5% heat inactivated fetal calf serum when compared to such an assay without said antibody has improved properties in antitumor therapy.

一种已经提高了抗肿瘤治疗的特性的抗体,所述抗体结合IGF-IR并且抑制IGF-I和IGF-II与IGF-IR结合,其特征在于所述抗体a是IgG1同种型,b显示其对IGF-I与IGF-IR结合的抑制的IC 50 值与其对IGF-II与IGF-IR结合的抑制的IC 50 值的比率为1∶3-3∶1,c当与没有所述抗体的这种测定比较时,其在5nM的浓度上,在包含0.5%的热灭活胎牛血清的培养基中,使用3T3细胞的细胞磷酸化测定中,抑制至少80%的IGF-IR磷酸化,所述3T3细胞提供400,000-600,000分子IGF-IR/细胞,和d当与没有所述抗体的这种测定相比,在包含0.5%的热灭活胎牛血清的培养基中,使用3T3的细胞磷酸化测定中,其在10μM的浓度上没有显示作为IGF-IR磷酸化所测量的IGF-IR刺激活性,所述3T3提供400,000-600,000分子IGF-IR/细胞。

The main research work of this dissertation is as follows: Based on the chemical reaction engineering theory and the nitrobenzene electroreduction mechanism, the plate and frame electrolyzer was designed and applied to the process of electroreduction nitrobenzene to p-aminophenol. This dissertation measured the residence time distribution data of the electrolyzer by means of the pulse response method and studied the rule of flow pattern along with the current capacity change. Under different conditions ,this dissertation studied the cyclic voltammetry properties of nitrobenzene on different electrodes by means of the dynamic cyclic voltammetry method and the electrode materials applied to the NB electroreduction have been selected primarily.Baseed on the results of cyclic voltammetry tests, this dissertation used p-electrode systems to measure the steady-state- polarization curves of nitrobenzene on different electrodes in H-type diaphragm cell, and obtained each primary factor s influence rule and the exchange current density value of each electrode.And then on the basis of the conclusions of fundamental researchs upword, the effects of influence factors on the the yield of p-aminophenol and the current efficiency,such as electrode material, current density, quantity of electricity circulated, nitrobenzene concentration . sulpuric acid concentration and so on, have been studied in detail in the systems of hign temperature , strong acidity and oxygen-poorthrough a series of electrolysis experiments in this paper.After all using Pb as anode Monel metal as cathode Dupont Nafion 417 cation-exchange membrane as membrane, this dissertation obtained the optimum technological condition: reaction temperature about 85C, current density 500A m-2, sulphuric acid concentration 20%wt.

论文的主要研究工作为:运用化学反应工程理论,结合硝基苯的电还原机理,设计出用于硝基苯直接电还原合成对氨基苯酚实验的板框式电解槽,并利用脉冲响应法测定了该板框式电解槽的停留时间分布数据,研究了流型随流量变化的规律;通过动态循环伏安法研究了硝基苯在不同电极上、不同条件下的循环伏安特性,初步评选出了用于硝基苯电还原的电极材料;结合循环伏安的测定结果,在H型隔膜电解槽中采用三电极体系测定了硝基苯在不同电极上、不同条件下的稳态极化曲线,得到了各主要因素的影响规律及硝基苯在各个电极上电还原的交换电流密度数值;在基础研究结论指导下,采用板框式电解槽,在高温、强酸、贫氧系统中,进行了一系列的电解实验,分别考察了电极材料、电流密度、通电量、硝基苯浓度、硫酸浓度等因素对收率及电流效率的影响,最终选择以蒙乃尔合金电极作为阴极、铅合金为阳极、Dupont Nofion 417阳离子交换膜为隔膜,得到由硝基苯直接电还原制对氨基苯酚的最佳电解工艺条件:反应温度85℃,电流密度500A·m~(-2),硫酸浓度20%wt。

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If you have any questions, you can contact me anytime.

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