卵清蛋白

方法作者用卵清蛋白免疫和激发SD大鼠。

Methods SD rats were immunized and challenged by chicken ovalbumin ( OVA ) .

结果表明，这种双敏感智能凝胶膜可以分别通过控制温度和pH值的变化，有效地控制纯水通量和卵清蛋白的截留率。

The results show that the flux of pure water and the rejection of ovalbumin are controlled effectively through adjusting temperatures and pH.

纳米粒治疗组上述3种指标均显著低于卵清蛋白致敏激发组和裸DNA组小鼠（P<0.01或P<0.05）。

Compared with OVA group and DNA group , those indexes in nanoparticle group were significantly decreased ( P < 0.01 or 0.05 ) .

卵清蛋白糖肽对hCG信号转导系统的抑制作用

Inhibition of ovalbumin glycopeptides on the hCG signal transduction system

而卵清蛋白致敏激发并给予裸DNA组与卵清蛋白致敏激发组比较差异无显著性，表明裸DNA难以通过气道内注入在活体动物气道表达。

There is no significant difference between OVA group and DNA group , indicating that bare DNA is hard to express in the animals via airway .

hCG受体的结合特性及卵清蛋白的抑制作用

Characterization of binding property to hCG receptor and inhibition effect of ovalbumin glycopeptides

卵清蛋白（OVA）制成哮喘模型，观察各组SOD、MDA水平的变化。

Egg albumen was used to make asthma models to observe the changes of SOD and MDA level .

除溶菌酶和牛血清白蛋白的吸附近似呈线性外，细胞色素－c、肌红蛋白、胰岛素、α－淀粉酶和卵清蛋白均呈凸型吸附。

It was found the adsorption isotherms of lysozyme and bovine serum albumin to be linear and those of cytochrome-c , myoglobin , insulin ,α - amylase , and ovalbumin to be convex .

哮喘组以鸡卵清蛋白（OVA）致敏和激发哮喘，对照组以生理盐水代替OVA进行致敏和激发。

Asthma models were established by sensitization and challenge with ovalbumin ( OVA ) .

基于Cre重组酶体系的鸡卵清蛋白基因打靶载体的构建

Construction of chicken ovalbumin gene targeting vector containing the Cre recombinase recognition site

用变性的琼脂糖凝胶电泳对各纯化步骤的核酸样品进行组成分析，确定出鸭卵清蛋白mRNA的大小约为21S。

The size of the duck ovalbumin mRNA characterized by denaturing agarose gel electrophoresis was 21s .

分别用碳二亚胺法和混合酸酐法制备诺氟沙星与卵清蛋白（OA）的结合物，作为诺氟沙星酶联免疫测定用的包被抗原。

The conjugates of norfloxacin-ovalbumin ( OA ) used for coating antigen were synthesized by carbodiimide method and mixed anhydride method , respectively .

采用卵清蛋白（ovalbumin，OVA）致敏和激发诱导小鼠变应性鼻炎。

The allergic rhinitis in mice was induced by sensitizing and challenging with ovalbumin ( OVA ) .

用国产蚕蛹蛋白粉喂养断奶SD大白鼠，以卵清蛋白粉作对照。

The baby SD rats were raised respectively for20 days with feed containing silkworm pupa protein powder (" SPP ") or egg white protein powder (" EWP ") .

方法以鸡卵清蛋白（OVA）致敏和雾化吸入刺激BALB/c小鼠以诱发EOS在气道聚集后将其分离纯化。

Methods BALB / c mice were sensitized and challenged by ovalbumin to recruit the aggregated eosinophil in the airways .

通过观察冷冻干燥海藻酸凝胶的断面扫描电镜（SEM）照片与卵清蛋白从海藻酸凝胶中的释放试验，分析了海藻酸凝胶性质对蛋白质在凝胶中扩散的影响。

By the scanning electron microscopy ( SEM ) micrograph and the release experiments , the effect of the characteristic of alginate gel on the release of ovalbumin from alginate beads was investigated .

采用圆二色谱（CD）、X射线衍射（XRD）、ANS荧光探针和紫外（UV）光谱研究了动态超高压微射流对卵清蛋白微观结构的影响。

The effect of dynamic high pressure microfluidization on the microstructure of ovalbumin was studied by CD spectra , XRD spectra , ANS fluorescence probe emission spectra and UV absorption spectra .

基于Box-Behnken模型的卵清蛋白糖基化制备技术

Optimization of the Preparation of Glycated Egg White Protein by Box-Behnken Model

鸡卵清蛋白基因启动子调控GFP基因在鸡原代输卵管上皮细胞和中国仓鼠卵巢细胞的表达

GFP Reporter Gene under the Direction of Chicken Ovalbumin Gene Promoter Expressed in the CHO Cell and in the Primary Cell Cultures of Chicken Oviduct

结果显示，T-2HS能与牛血清白蛋白（BSA）和卵清蛋白（OVA）结合生成T-2毒素抗原。

The result showed that T-2 toxin could conjugate with BSA or OVA to produce T-2 toxin antigen .

方法卵清蛋白（OVA）致敏并激发Balb/c小鼠建立急性哮喘模型。

Methods Sensitized Balb / c mice were challenged by ovabumin ( OVA ) to establish the acute asthmatic mo - ( del ) .

本研究分别以牛血清白蛋白（BSA）、卵清蛋白（OVA）为蛋白质载体，采用碳二亚胺法（CDI）将半抗原青霉素钠（PEN）分别与BSA、OVA偶联，合成了完全抗原PEN-EDC-BSA和PEN-EDC-OVA。

In this study penicillin hapten was respectively coupled with BSA and OVA to synthesize PEN-EDC-BSA and PEN-EDC-OVA complete antigen applying CDI .

用活性酯和混合酸酐法将半抗原2,4-D分别与牛血清白蛋白（BSA）和卵清蛋白（OVA）共价偶联；

Hapten 2,4-D was covalently attached to bovine serum albumin ( BSA ) and ovalbumin ( OVA ) using the modified active ester method and the mixed-anhydride method , respectively .

目的：观察小鼠哮喘模型气道卜皮内肥大细胞的数量，进一步阐明肥大细胞在鸡卵清蛋白（OVA）诱导的小鼠哮喘模型中的作用。

Objective : To investigate the number of mast cells and clarify the possible role of mast cells in the development of ovalbumin ( OVA ) - induced asthma model in vivo .

结果；在接种卵清蛋白的小鼠的肺中应用微点阵分析表明，CD48因子（表达）上调。

Measurements and Main Results : Microarray data analysis demonstrated upregulation of CD48 in the lungs of OVA-challenged mice .

采用5′RACE方法确定鸡卵清蛋白基因转录起始点的位置，通过序列分析得出转录起始点为G，从而确定出核心启动子及上游调控区的位置。

To determine the core promoter of chicken ovalbumin gene and 5 ′ upstream regions , the transcription initiation site of ovalbumin gene was confirmed by 5 ′ RACE method , at the same time , the regulatory elements of chicken ovalbumin gene were determined by sequence analysis .

以卵清蛋白（OVA）致敏激发建立哮喘模型，于OVA致敏前及后5d分别以BCG皮内注射干预。

The mouse were sensitized and challenged with ovalbumin ( OVA ) to establish asthmatic model . The mouse in BCG treatment group were injected intradermally with BCG 5 days before and after sensitization .

采用4%卵清蛋白生理盐水和4%氢氧化铝凝胶致敏，卵清蛋白复制哮喘模型，放射免疫法测定血清总IgE的含量；生物定量法测定血浆中血小板活化因子（PAF）的含量。

Determine the general serum IgE contents of guinea pigs by radioimmunoassay and the plasma platelet activating factor ( PAF ) contents by biologically quantitative method after GDC treated guinea pigs ' asthmatic model making and reproducing .

实验还对蛋白芯片检测阿特拉津进行了条件优化，其抗体固定化时间为2h，用卵清蛋白为封闭液的封闭时间为1h，样品稀释液pH值为8.0。

The detection of atrazine and papaverine was performed qualitatively and quantitatively under the optimized conditions which includes antibody immobilized time ( 2h ), blocking buffer containing OVA and blocking time ( 1h ) , sample buffer pH value ( pH 8.0 ) .

以卵清蛋白（ovalbumin，OVA）诱导小鼠特应性皮炎为动物模型，研究美能对其血清IgE、腹部真皮炎症细胞浸润和血清某些细胞因子IL-2、IL-4、IFN-γ的影响。

Ovalbumin-induced murine dermatitis was used as an animal model . The effect of glycyrrhizin on dermal inflammatory infiltration cell count of the abdomen and serum level of IgE , IL-2 , IL-4 and IFN - γ were examined .