The green fluorescence protein (GFP) gene recombinant virus labeling is a new method for the neuroanatomical studies.
绿色荧光蛋白（GFP）基因重组病毒标记技术是神经解剖研究的新方法。
Objective: to construct enhanced cyan fluorescence protein (ECFP) lentiviral vector using the gene multipoint mutation.
目的：通过多点突变构建增强型青色荧光蛋白(ECFP)慢病毒表达载体。
We used gel retardation assay experiment and green fluorescence protein marker to investigate their transfer efficiency.
用电泳实验和绿色荧光蛋白标记方法研究了它的转染效率。
The results show that the fluorescence resuming ratio is proportional to the concentration of target protein.
实验结果表明，荧光恢复程度与靶蛋白的浓度正相关。
The fluorescence of the phosphorylated protein is normalized to that of the total protein in each well to correct for well-to-well variations.
磷酸化蛋白的荧光按照同一孔中的总蛋白被标准化，以纠正孔间的差异。
Fluorescence spectroscopy is an effective method of study on protein conformation in aqueous solution.
萤光光谱法是研究蛋白质在水溶液中分子构象的一种有效方法。
Objective To assess the value of two-color infrared fluorescence imaging system in detecting protein phosphorylation in comparison with chemiluminescent detection.
目的通过与化学发光法比较，了解双色红外荧光技术在目标蛋白磷酸化检测中的优势。
The fluorescence indicates the amount of mechanical stress in the host protein and this can be imaged in different parts of a cell or an organism.
荧光显示的是宿主蛋白的机械应力，这可以显示细胞或机体的不同部位的影像。
In the second section, a chip based ce system with laser induced fluorescence detector was developed to achieve the separation of protein and polypeptide.
在第二章中，采用激光诱导荧光检测芯片毛细管电泳系统进行蛋白质和多肽分离的研究。
Inherent ultraviolet absorption spectrum and fluorescence spectrum of protein can be used in protein analysis, but the sensitivity of these methods can not meet the demand of micro determination.
蛋白质内源紫外吸收光谱和荧光光谱可以用于蛋白质分析，但其灵敏度不能满足微量分析的要求。
Meanwhile, the secondary structure of membrane protein was destroyed and endogenous fluorescence decreased.
同时，膜蛋白二级结构遭到破坏，内源荧光下降。
Fluorescence analysis reveals that soybean protein are modified by high pressure to have larger hydrophobic regions.
荧光分析表明，豆浆中大豆蛋白的表面疏水区域随处理压力的升高和处理时间的延长而增加；
Then they were used as a kind of protein probe. The binding constant of carboxylic metal phthalocyanine with BSA was determined by fluorescence spectroscopy method.
以羧基酞菁金属配合物为荧光探针，采用荧光光谱法求出羧基酞菁金属配合物与BSA的结合常数。
The methamidophos can quench the fluorescence of membrane protein.
甲胺磷对血影膜的荧光有强烈的猝灭作用。
The membrane was also titrated with AAP by measuring the intrinsic fluorescence of protein.
用AAP滴定红细胞膜，测蛋白质自身荧光变化。
The fluorescence of rice protein also enhanced.
蛋白质荧光强度增强。
This paper reports the application of fluorescence anisotropy technique to the (assay) of proteases via a protein substrate labeled with tetramethyl isothiocyanate rhodmine(TMRITC).
建立了一种基于荧光各向异性原理均相测定蛋白酶及其抑制剂的方法。
In a further embodiment, adding the protein labeled with the label on the label and fluorescence reagent combination to the purpose of specific marker proteins.
在进一步的实施方案中，添加可以与带标签的蛋白质上的标签结合的标签结合荧光试剂，以特异性标记目的蛋白质。
The quenching mechanism of DNAF on intrinsic fluorescence quenching of protein and the types of interaction forces were proposed.
研究了DNAF对蛋白质内源荧光猝灭的猝灭机制和主要作用力类型。
The separated protein is laser induced fluorescence detected and marked with fluorescent dye.
蛋白质分离后用激光诱导荧光检测，蛋白质用荧光染料进行标记。
Saliva protein molecules are in combination with EGCG form compound so that the saliva protein fluorescence quenching in solution.
唾液蛋白质分子与EGCG结合形成复合物使唾液蛋白质荧光猝灭。
The expression of HGF protein was observed by fluorescence microscopy and immunohistochemistry.
用荧光显微镜以及免疫组织化学方法观察HGF表达情况。
Protein-like fluorescence peak intensity began to increase in early winter and spring, and the summer reached to the peak.
类蛋白荧光峰的强度在年初冬季和春季开始升高，夏季达到最高。
The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.
用改良的考马斯亮蓝法对硅片和改性后的硅片进行了蛋白质吸附研究，并采用荧光显微镜观察了胎鼠海马神经细胞在改性前后硅表面的黏附行为。
The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.
用改良的考马斯亮蓝法对硅片和改性后的硅片进行了蛋白质吸附研究，并采用荧光显微镜观察了胎鼠海马神经细胞在改性前后硅表面的黏附行为。
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