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This study was based on the soy protein isolates as raw materials. Chemical modification( acetylation,succinylation ,phosphorylation and urea modification) of SPI were used to improve adhesive strength and water resistance of SPI-based plywood adhesives. Then two modified ways combined were applied to SPI and their adhesive properties were studied. This research also characterized the thermal and adhesive properties of two major soy protein components 7S conglycinin and 11S glycinin after urea modification. Finally, the mechanism of improving SPI's adhesive properties was preliminarily discussed.

本文是以大豆分离蛋白为原料,进行SPI的化学修饰以提高其胶粘特性;采用了磷酸化试剂三聚磷酸钠、乙酰化试剂乙酸酐、琥珀酰化试剂琥珀酸酐和有机溶剂尿素修饰和变性SPI,研究修饰和变性后的SPI作为木材胶粘剂的胶粘性与耐水性,同时研究了两种方法复合修饰SPI对其粘度、胶粘强度和耐水性的影响;然后以SPI为原料,进行7S和11S球蛋白的提取以及胶粘特性的研究,对SPI起胶粘特性的机理进行了初步探讨。

Methods Before and 30 days after treatment with histotherapy,T lymphocyte subpopulation,complement and complement activation segment were measured in 17 patients by ELISA and APAAP techniques.

方法采用ELISA法和碱性磷酸酶抗碱性磷酸酶法,观察17例银屑病病人采用组织疗法治疗前及治疗30d后外周血T淋巴细胞亚群补体及活化片段的变化,同时观察了组织疗法的效果。

PartⅡThe mechanism elucidation about effects ofα-(2,3)/(2,6)sialic acid on the Cx43gap-junction functions.(1) Westernblotting experiment showed that the decrease of sialic acid didn\'t changethe Cx43 expression and its phospholation level.(2) Westernblotting experiment showed sialidase didn,t change the ZO-1 expression,IP and confocal experiment showed sialidase improved the interaction of Cx43 andZO-1.(3) Westernblotting experiment showed sialidase didn\'t change N-cadherin expression,IP and confocal experiment showed sialidase promoted the complex formation ofCx43 and N-Cadherin.(4)Sialidase could increase the ERK1/2 phospholation level,and enchanedintercellular homotypic adhesion,Immunofluorometric assay showed sialidase couldpromote the N-cadherin cluster on the membrance.

第二部分:α—(2,3)/(2,6)唾液酸对肿瘤细胞CX43间隙连接功能影响的机制研究1、Westernblotting结果表明降低细胞膜表面唾液酸并不改变Cx43的表达及其磷酸化水平:但Cx43连接斑形成增多;2、Westernblotting结果表明唾液酸酶作用后细胞ZO—1表达没有改变,IP及免疫荧光共定位结果表明唾液酸酶作用后促进了Cx43与ZO-1的结合;3、Westernblotting结果表明唾液酸酶作用后细胞N-cadherin表达没有改变,IP及免疫荧光共定位结果表明唾液酸酶作用后促进了Cx43与N-Cadherin复合物的形成;4、唾液酸酶作用后细胞内ERK1/2磷酸化水平明显增加,细胞间同质粘附增加,以及免疫荧光表明唾液酸降低后可促进N-cadherin的膜成簇。

The influences of reaction time, pH, and the concentrations of phosphate on the adsorption of phosphate on hydrotalcite arid its calcined products were studied.

研究了反应时间、声及磷酸根浓度对磷酸根在水滑石及其焙烧产物上吸附量的影响。

A new synthesis method of Taxane s was reported involving radicals generated from hypophosphorous acidn initiated by 2,2′-azobisisobutyronitrile.

由偶氮二异丁腈引发次磷酸产生次磷酸根自由基,以链式自由基反应机制脱除紫杉烷类化合物结构中的含氧基团,简单、高效地合成了紫杉烷。

A new synthesis method of Taxanes was reported involving radicals generated from hypophosphorous acid n initiated by 2,2′-azobisisobutyronitrile.

由偶氮二异丁腈引发次磷酸产生次磷酸根自由基,以链式自由基反应机制脱除紫杉烷类化合物结构中的含氧基团,简单、高效地合成了紫杉烷。

Animal models were worked out by injecting granule solution into the lung of mice through trachea to study pulmonary lesions in mice. All mice were intratracheally instilled every three days. At the tenth day, mice were sacrificed and. Lung organ coefficient, albumin, total protein, acid phosphatase and Alkaline phosphatase were measured.

为研究纳米二氧化钛对小鼠肺部的损伤,将小鼠采用非暴露式气管内注入法注入颗粒悬液建立动物模型,每隔2d染毒一次,在第10d处死小鼠,测定肺脏器系数及肺部组织中白蛋白、总蛋白、酸性磷酸酶和碱性磷酸酶的含量。

Chromatographic fingerprint index F and chromatographic fingerprint relative index Fr were used as the objective functions for the evaluation,and the extract of Saussurea involucrate by water was used as the sample.

以色谱指纹图谱指数F和色谱指纹图谱相对指数Fr作为评价毛细管电泳分析系统的目标函数,以雪莲药材水提取液为样品,考察一定浓度的硼砂、硼酸、磷酸氢二钠和磷酸二氢钠溶液按三角形优化法和四面体优化法构成背景电解质时对样品的分离情况,通过添加有机改性剂和调节pH进行再优化。

Nineteen spots were changed significantly after FA treatment.Thirteen proteins were identified by peptide mass fingerprinting or peptide sequence analysis,including putative nucleoside diphosphate kinase,elongation factor 1-gamma,triosephosphate isomerase,60S acidic ribosomal protein P0,heat shock protein 75 kDa,similar to heat shock 70kD protein binding protein,annexin I,hypothetical protein FLJ34423,microtubule-actin crosslinking factor 1,lamin B2,ATP synthase alpha chain,mitochondrial precursor,proteasome subunit alpha type 6.These identified proteins involved in energy metabolism,translation and RNA processing,protein folding,redox regulation,cell structure and cell signaling.

双向凝胶电泳结果显示,甲醛刺激后19个蛋白斑点发生变化,肽指纹图谱及肽序列标签鉴定了其中13个蛋白斑点,已鉴定的蛋白包括二磷酸核苷酸激酶、延长因子1-γ,磷酸丙糖异构酶、60S酸性核糖体蛋白P0、75kDa热休克蛋白、70kD热休克蛋白样结合蛋白、钙依靠磷脂结合蛋白I、假想蛋白FLJ34423、微管-肌动蛋白交叉连接因子1、核纤层蛋白B2、ATP合成酶α链、蛋白酶体α亚基6,这些蛋白功能涉及转录调节、蛋白折叠、信号传导、能量代谢、细胞骨架等各个方面。

Thirteen proteins were identified by peptide mass fingerprinting or peptide sequence analysis,including putative nucleoside diphosphate kinase,elongation factor 1-gamma,triosephosphate isomerase,60S acidic ribosomal protein P0,heat shock protein 75 kDa,similar to heat shock 70kD protein binding protein,annexin I,hypothetical protein FLJ34423,microtubule-actin crosslinking factor 1,lamin B2,ATP synthase alpha chain,mitochondrial precursor,proteasome subunit alpha type 6.These identified proteins involved in energy metabolism,translation and RNA processing,protein folding,redox regulation,cell structure and cell signaling.

双向凝胶电泳结果显示,甲醛刺激后19个蛋白斑点发生变化,肽指纹图谱及肽序列标签鉴定了其中13个蛋白斑点,已鉴定的蛋白包括二磷酸核苷酸激酶、延长因子1-γ,磷酸丙糖异构酶、60S酸性核糖体蛋白P0、75kDa热休克蛋白、70kD热休克蛋白样结合蛋白、钙依赖磷脂结合蛋白I、假想蛋白FLJ34423、微管-肌动蛋白交叉连接因子1、核纤层蛋白B2、ATP合成酶α链、蛋白酶体α亚基6,这些蛋白功能涉及转录调节、蛋白折叠、信号传导、能量代谢、细胞骨架等各个方面。

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