Conclusion: It can provide reference for identifying and distinguishing Radix Polygalae from different provenances to use allozyme and soluble protein gel electrophoresis technology.
结论：利用等位酶与可溶性蛋白凝胶电泳技术可为不同种源远志的鉴定与划分提供参考。
Objective: By protein gel electrophoresis, to seek the differences between the meridian course and the non-meridian part in rat, to confirm whether there is any special protein in the meridian course.
目的：通过蛋白质凝胶电泳技术，寻找大鼠循经部位与非循经部位蛋白质条带的差异，证实循经部位是否存在特异蛋白。
The electrophoertograms of protein and alkaline phosphatase isoenzymse. of serum in black pig were analysed by disc polyacrylamide gel electrophoresis method.
用聚丙烯酰胺凝胶圆盘电泳分析了黑猪血清蛋白质和碱性磷酸酶同工酶生化位点多态性的分布。
Method: Gel electrophoresis of soluble protein.
方法：可溶性蛋白质凝胶电泳。
Two dimensional polyacrylamide gel electrophoresis(2D PAGE) followed by mass spectrometry(MS) is the most widely used method of protein resolution and identification. But it exist shortcomings.
双相聚苯稀酰氨凝胶电泳（2DPAGE）与质谱（MS）是分辨和鉴定蛋白的最常用的方法，但也存在有缺点。
Methods EOLA1 protein was expressed in vitro through couple transcription and translation. The products were detected by gel electrophoresis.
方法通过偶联转录翻译系统体外表达EOLA1蛋白，并用变性凝胶电泳进行产物检测；
The protein composition of sericin have been studied by polyacrylamide gel electrophoresis.
用聚丙烯酰胺凝胶电泳法研究丝胶的蛋白质组成问题。
Objective to establish the normal reference values of serum protein with agarose gel electrophoresis (AGE) in local clinical laboratory.
目的制定本实验室琼脂糖凝胶电泳法(age)测定血清蛋白的正常参考值范围。
The qualitative patterns of protein synthesis in nuclear transplant rabbit embryos were examined by SDS-polyacrylamide gel electrophoresis followed by silver staining.
采用SDS-聚丙烯酰胺凝胶电泳及银染法，对兔核移植胚胎蛋白质合成类型的变化进行了研究。
Double diffusion method, Westergren and automatic gel method detected ant-SSA and ant-SSB antibody, ESR and serum protein electrophoresis respectively.
抗SSA和抗SSB抗体、ESR、血清蛋白电泳检测分别采用免疫双扩散法、魏氏法、全自凝胶法。
Methods: Based on several reported SDS-PAGE systems for low molecular weight protein, the buffer systems, concentrations of separating gel and stacking gel, electrophoresis procedures were optimized.
方法：比较以往报道的各种低分子量蛋白的电泳分离方法，对电泳缓冲液系统、分离胶和浓缩胶的浓度、电泳程序等进行了优化。
The difference of this chapter is that we use an optimized one-dimensional gel electrophoresis and liquid chromatography tandem mass spectrometry combined protein mixture identification technology.
所不同的是我们采用了优化的一维凝胶电泳和液相色谱串联质谱联合的复杂蛋白质混合物鉴定技术。
The experimental procedures of agarose gel electrophoresis for detecting urinary protein were improved, and the LDH isoenzymes and lipoproteins could be analysed simultaneously.
本文对尿蛋白琼脂电泳法进行了改进，可以与L DH同二酶、脂蛋白同步电泳。
The result of polyacrylamide gel electrophoresis shows that the protein band of expression is found at the position of about 55kd.
聚丙烯酰胺凝胶电泳实验结果表明在大约55kd的位置上有表达的蛋白质条带。
Method Gel electrophoresis of soluble protein was used.
方法可溶性蛋白质凝胶电泳。
Two methods, high performance liquid chromatography and gel electrophoresis (SDS-PAGE), were used to evaluate the influence of different dyes'structures on protein labeling.
同时应用高效液相色谱和聚丙烯酰胺凝胶电泳（SDS-PAGE）两种分析技术研究染料结构对蛋白质标记的影响。
Objective To explore an optimal cartilage protein extraction approach that can guarantee both the image quality and the result fidelity of the two-dimensional gel electrophoresis (2-DE) technique.
目的探索可兼顾双向电泳凝胶图像质量和结果保真性的软骨蛋白提取方案。
Study protein-protein interaction by native and denaturing gel electrophoresis, western blotting, and immunology precipitation.
研究蛋白质-蛋白质相互作用，由本地和变性凝胶电泳免疫印迹，免疫沉淀。
The SDS gel electrophoresis analysis shows that the expression of EPSPS recombined protein is over 55% and the purified EPSPS recombined protein reached as 90%.
SDS电泳分析结果表明EPSPS重组蛋白的表达量在55%以上，纯化的EPSPS重组蛋白纯度可以达到90%。
The laboratory has research facilities such as PCR, Gel Imager System, Protein Electrophoresis, Nucleic Acid Electrophoresis and High-speed Refrigerated Centrifuge.
该室拥有PCR仪、凝胶成像仪、蛋白质电泳仪、核酸电泳仪、高速冷冻离心机等研究设备。
The laboratory has research facilities such as PCR, Gel Imager System, Protein Electrophoresis, Nucleic Acid Electrophoresis and High-speed Refrigerated Centrifuge.
该室拥有PCR仪、凝胶成像仪、蛋白质电泳仪、核酸电泳仪、高速冷冻离心机等研究设备。
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