• The collagen molecular weight and structure were analyzed by SDS PAGE.

    通过SDS-PAGE试验,分析酸溶性胶原分子量基本结构

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  • A 190kd protein of motoneurons was isolated from the anterior roots of human spinal cord by SDS PAGE.

    本研究采用SDS凝胶电泳方法脊神经分离出人脊髓前角运动神经元特有蛋白—190kd

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  • The purified product was analyzed by SDS PAGE and the amount of target protein calculated by gray scanning.

    采用SDS PAGE分析纯化后目的蛋白将蛋白电泳条带进行灰度扫描,计算目的蛋白的含量

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  • Expressed protein was analyzed with SDS PAGE. Hemolysin test was performed to determine the hemolysis activity.

    SDS PAGE分析蛋白表达溶血试验检测表达蛋白的溶血活性。

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  • Methods The soluble antigens of the parasites were analysed by means of SDS PAGE and two dimensional gel electrophoresis.

    方法SDS-PAGE和双向电泳方法,日本血吸虫两性成虫全可溶性抗原进行分析。

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  • Results SDS PAGE and thin layer scanning showed that the expressed product contained about 6.4% of total somatic protein.

    结果SDS PAGE扫描分析表明,外源蛋白表达菌体裂解蛋白总量6 . 4 %。

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  • SDS PAGE analysis demonstrated that the enzyme was produced to the extent of as much as 38% of the total cellular protein.

    SDS PAGE分析表明,鸡肌腺苷酸激酶含量可占大肠杆菌细胞蛋白含量的38%。

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  • After determining the molecular weight of the purified protein by SDS PAGE, the band was excised from gel for protein identification.

    SDS PAGE测定纯化蛋白分子量,然后切下目的蛋白条带,进行蛋白质鉴定

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  • The double immunodiffusion test and ELISA were used to test the titer of the antiserum. The specificity of antibody was detected by SDS PAGE and ELIB (Enzyme linked immune blotting).

    采用多途径免疫法制备单特异性血清,琼脂扩散试验ELISA测定抗体价,SDS PAGEELIB检测抗体特异性。

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  • Methods nuclear matrix proteins were extracted under high salt extraction procedures, and changes of nuclear matrix proteins were analysed by SDS PAGE and two dimensional (2d) electrophoresis.

    方法应用提取法抽提细胞核基质蛋白SDS PAGE电泳(2d)法分析白血病细胞正常骨髓细胞核基质蛋白变化

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  • The strategies of quality improvement and theuses of SDS-PAGE in wheat breeding programmes were discussed.

    本文还品质改良策略SDSPAGE育种实践中的应用进行了讨论。

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  • According to the analysis of SDS-PAGE, the bands of the graft subunits decreased and the glycosyl bands were seen more clearly with the degree of graft (DG) increasing.

    聚丙烯凝胶电泳(SDS - PAGE)分析结果表明,随着(DG)增加,接枝物的基谱逐渐减少,糖基谱带变得明显

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  • Analyse the protein difference of purification process Through SDS-PAGE.

    PAGE分析纯化过程蛋白质组成差异

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  • Then, antigen was prepared by conjugation of hapten with carrier protein by carbodiimide (EDPC) method and was identified by UV spectroscopy and SDS-PAGE.

    然后通过碳二亚胺将半抗原载体蛋白偶联制备人工抗原,采用紫外扫描SDS - PAGE鉴定

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  • Recombinant human BDNF was expressed in E. coli and is supplied in a lyophilized form. A greater than 96% purity was determined by reverse phase-HPLC and SDS-PAGE.

    重组人脑源性神经营养因子(BDNF)大肠杆菌中表达冻干形式提供相高效液相色谱法和SDS-PAGE测定其纯度大于96%。

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  • The types, distribution and histochemistry characters of mucous cells of Meretrix meretrix Linnaeus were studied by histological and histochemical methods and SDS-PAGE electrophoresis.

    运用组织学、组织化学聚丙烯酰胺凝胶电泳技术,研究了文蛤粘液细胞类型分布组化特性

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  • Results: (1) Molecular quantity of the purified flagellin was about 65kd by SDS-PAGE electrophoresis.

    实验结果:(1)纯化鞭毛蛋白sDS - PAGE电泳,分子量为65kd

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  • The 7s and 11s globulin content of 5 soybean varieties grown in 11 locations of Heilongjiang province, Jilin province and Liaoning province were analysed with the line gradient SDS-PAGE.

    利用线性梯度SDS - PAGE方法分析东北地区(黑龙江省吉林省辽宁省)11地点5个大豆品种7s和11s球蛋白含量

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  • The fraction of vegetative storage protein(VSP) in different parts of Ginkgo biloba and its annual dynamic changing rules were studied by the technology of SDS-PAGE and microscope.

    采用SDS-聚丙烯酰胺凝胶电泳技术电子显微技术,银杏不同部位营养贮藏蛋白质组分及其动态变化规律进行了研究

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  • Every collected peak was identified by SDS-PAGE after purified with gel chromatography by fast protein liquid chromatography system.

    结合物快速蛋白质液相系统凝胶色谱纯化SDS PAGE鉴定收集

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  • Method: Use the method of indirect immunofluorescence, mice cross protection test and SDS -page to determine the serum type, the toxicity and the protein atlas of the isolated strains.

    方法采用间接免疫荧光法小鼠保护试验以及SDS -聚丙烯胺电泳法,分别测定分离株血清类型毒力蛋白图谱

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  • SDS-PAGE and scanning monitor were used to detect expression efficiency and analyze the solubility of protein.

    采用SDS - PAGE岛津薄层扫描分析仪进行表达效率检测、蛋白可溶性扫描分析

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  • SDS-PAGE was used to analyze proteolysis of dry-salted duck samples of different processing phases and the free-amino acid(FAA) were tested as well.

    SDS-PAGE电泳分析蛋白质降解规律,同时比较加工初期及末期游离氨基酸变化,并以不接菌样品对照。

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  • The high molecular weight glutenin subunits and their encoding genes in Aegilops variables were characterized by SDS-PAGE and molecular cloning.

    利用SDS-PAGE分子克隆方法研究了易山羊草的分子量谷蛋白亚基及其基因

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  • The purity of isolated VLDL and LDL was confirmed by the lipoprotein electrophoresis on agarose gel and PAGE and by the apolipoprotein electrophoresis on SDS-PAGE.

    所得极低密度脂蛋白VLDL低密度脂蛋白(LDL琼脂电泳、聚丙烯酰胺电泳(PAGE)及脂蛋白SDS-聚丙烯酰胺电泳(SDS-PAGE)鉴定纯度良好。

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  • Method Type I collagen was attained from rat tail tendon with method of acid extraction, then undergone analysis and identification using ultraviolet spectroscopy, SDS-PAGE and IEF.

    方法采用提法肌腱提取I胶原蛋白,并用紫外扫描法、SDS - PAGEIEF进行分析鉴别

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  • SDS-PAGE is an effective method for protein analysis, comparison and characteristic identification.

    PAGE蛋白质分析比较特性鉴定有效方法

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  • The high molecular weight glutenin subunit(HMW-GS) of 136 local germplasms was analyzed by SDS-PAGE to screen better germplasm resources for quality improvement of wheat in Guizhou.

    为了筛选优良种质资源应用于小麦的品质改良,利用SDS-PAGE技术贵州省的136份地方种质进行分子量麦谷蛋白亚基组成分析。

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  • The high molecular weight glutenin subunit(HMW-GS) of 136 local germplasms was analyzed by SDS-PAGE to screen better germplasm resources for quality improvement of wheat in Guizhou.

    为了筛选优良种质资源应用于小麦的品质改良,利用SDS-PAGE技术贵州省的136份地方种质进行分子量麦谷蛋白亚基组成分析。

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