The subunit molecular weight was determined as 32600 by SDS-PAGE.
用SDS-聚丙烯酰胺凝胶电泳测定亚基分子量为32600。
SDS-PAGE analysis suggested that the size of protein is about 59KD.
表达产物的SDS-PAGE分析表明，蛋白质分子量大小约为59KD。
Analyse the protein difference of purification process Through SDS-PAGE.
PAGE分析纯化过程中蛋白质组成的差异。
Objective To establish a quick and easy method for SDS-PAGE protein staining.
目的建立一种快速，简易的SDS-PAGE染色方法。
It was shown as a single band in SDS-PAGE. The molecular weight of lactoperoxidase was 75035d.
经SDS - PAGE测定，分离出的乳过氧化物酶显示为单一区带，相对分子质量为75035d。
SDS-PAGE is an effective method for protein analysis, comparison and characteristic identification.
PAGE是蛋白质分析、比较和特性鉴定的有效方法。
SDS-PAGE showed that OBPC and the four solubility fractions had different polypeptide compositions.
PAGE的结果表明OBPC及各蛋白组分有不同的分子组成。
Results: (1) Molecular quantity of the purified flagellin was about 65kd by SDS-PAGE electrophoresis.
实验结果：(1)纯化的鞭毛蛋白经sDS - PAGE电泳，分子量约为65kd。
The strategies of quality improvement and theuses of SDS-PAGE in wheat breeding programmes were discussed.
本文还对品质改良策略和SDS—PAGE在育种实践中的应用进行了讨论。
The 190kd protein of motor nerve was isolated from the anterior roots of human spinal cord by the SDS-PAGE.
采用SDS凝胶电泳方法从人脊神经前根中分离出运动神经元特有的蛋白组份190KD蛋白。
The obtained proteins were checked for the purity through SDS-polyacrylamide gel electrophoresis (SDS-PAGE).
用十二烷基硫酸钠-凝胶电泳(SDS - PAGE)和二维凝胶电泳鉴定蛋白质纯度。
SDS-PAGE and scanning monitor were used to detect expression efficiency and analyze the solubility of protein.
采用SDS - PAGE及岛津薄层扫描分析仪进行表达效率检测、蛋白可溶性的扫描分析。
After quantification, the protein samples were separated by isoelectric focusing electrophoresis and then by SDS-PAGE.
定量后，分别进行一维等电聚焦分离和二维聚丙烯酰胺凝胶电泳分离。
Every collected peak was identified by SDS-PAGE after purified with gel chromatography by fast protein liquid chromatography system.
结合物经快速蛋白质液相层析系统用凝胶色谱柱纯化后，用SDS PAGE鉴定各收集峰。
The proteins were analyzed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and capillary zone electrophoresis (CZE).
用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS - PAGE)和毛细管区带电泳(CZE)分析蛋白质的组分。
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和分子克隆方法研究了易变山羊草的高分子量谷蛋白亚基及其基因。
Analysis of SDS-PAGE and thin layer scanning results showed that amount of expressed fusion protein was 18.6% in total lysis protein of bacteria.
结果：SDS - PAGE和薄层扫描分析表明外源蛋白的表达量占菌体裂解蛋白总量的18.6%。
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.
用SDS-PAGE电泳分析蛋白质的降解规律，同时比较加工初期及末期游离氨基酸的变化，并以不接菌样品为对照。
Method nuclear matrix proteins were extracted under high-salt extraction procedures, and changes of nuclear matrix proteins were analysed by SDS-PAGE.
方法应用高盐抽提法抽提细胞核基质蛋白，SDS PAGE技术分析白血病细胞与正常骨髓细胞核基质蛋白的变化。
After SDS-PAGE, the recovery of CP added the same volume of incomplete Freund Adjuvant emulsified completely, injected rabbits by subcutaneous injection.
PAGE电泳后，将表达的CP蛋白切胶回收，研磨成粉后加入等体积的福氏不完全佐剂，乳化制备成抗原。
Then, antigen was prepared by conjugation of hapten with carrier protein by carbodiimide (EDPC) method and was identified by UV spectroscopy and SDS-PAGE.
然后通过碳二亚胺法将半抗原与载体蛋白偶联制备人工抗原，采用紫外扫描及SDS - PAGE鉴定。
Methods Casein was hydrolyzed by trysin and chyomtrysin together. The enzymatic hydrolysis was filtrated by ultrafiltrate membrane, and analyzed by SDS-PAGE.
方法将酪蛋白酶解，其酶解产物经超滤膜过滤，用十二烷基磺酸钠——聚丙烯酰铵凝胶电泳（SDS-PAGE）方法分析其酶解情况。
On SDS-polyacrylamide gel electrophoresis (SDS-PAGE)the eluate from the column with the McAb coupled showed a single band, corresponding to the elution peak.
聚丙烯酰胺凝胶电泳显示单抗偶联柱层析洗脱物仅有单一区带与洗脱峰对应；
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）在大肠杆菌中表达，以冻干形式提供。反相高效液相色谱法和SDS-PAGE测定其纯度大于96％。
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）及低密度脂蛋白（LDL）经琼脂糖电泳、聚丙烯酰胺电泳（PAGE）及载脂蛋白SDS-聚丙烯酰胺电泳（SDS-PAGE）鉴定纯度良好。
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，随着接枝度(DG)的增加，接枝物的亚基谱带逐渐减少，糖基谱带变得明显。
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和电子显微技术，对银杏不同部位的营养贮藏蛋白质组分及其动态变化规律进行了研究。
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.
方法采用酸提法从鼠尾肌腱中提取I型胶原蛋白，并用紫外扫描法、SDS - PAGE和IEF进行分析和鉴别。
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.
为了筛选优良的种质资源应用于小麦的品质改良，利用SDS-PAGE技术对贵州省的136份地方种质进行高分子量麦谷蛋白亚基组成分析。
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.
为了筛选优良的种质资源应用于小麦的品质改良，利用SDS-PAGE技术对贵州省的136份地方种质进行高分子量麦谷蛋白亚基组成分析。
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