冰冻切片的抗原也在第四周开始出现，定位在卵黄膜及卵壳上。
In the cryostat section, the antigens also appeared at the fourth week, they were localized on vitelline membrane and egg shell.
目的探讨不同抗体和透膜剂组合对流式细胞术中胞浆抗原检测的影响。
Objective To explore the effect of different panels of antibodies and permeabilizations on detection of intracellular antigens.
本文采用免疫转印技术分析了肝病患者血清与肝特异性膜脂蛋白（LSP）抗原性多肽成份的反应。
The reactions of sera from patients with liver diseases to the antigenic polypeptides of liver specific membrane lipoproteins (LSP) were studied with the immunoblotting technique.
抗KLH血清引起阳性的尾蚴膜反应但不引起阳性的环卵沉淀试验，与可溶性虫卵抗原的交互抑制试验结果表明二者的抗原性部份交叉。
Antisera against KLH induced positive CHR but not positive COP. The results of reciprocal inhibition experiment indicated that there is a partial cross antigenicity between KLH and SEA.
膜乳化-液中干燥法的条件比较温和，微胶囊化过程没有破坏灭活sars冠状病毒的抗原性。
The antigenicity of SARS virus was not destroyed in the encapsulation process because of the mild conditions of membrane emulsification-drying method in liquid.
目的研制针对人补体膜攻击复合物（MAC）新抗原的特异性单克隆抗体。
Objective To prepare monoclonal antibody (McAb) against neoantigen of the human complement membrane attack complex (MAC).
膜拥有统一的孔径，从而也就有了能用于可重复的进行抗原抗体结合的液固界面。
The membrane provides a uniform pore and, thus, a liquid–solid interface for reproducible antigen–antibody binding.
结论白癜风患者血清中存在抗mchr1的自身抗体，MCHR1是MC膜表面的白癜风相关抗原。
Conclusion There are anti-MCHR1 antibodies in sera of some patients with vitiligo. MCHR1 is one of vitiligo related antigen and it is located on melanocyte membrane.
在玻璃条和捕获膜之间加入一个反应垫，可以增强检测物抗体抗原结合物的形成。
The detection antibody-analyte complex formation is enhanced by inserting a reaction pad between the glass strip and the capture membrane.
CSFV囊膜糖蛋白E2是诱导中和抗体及激发保护性免疫应答的主要抗原蛋白。
Envelope glycoprotein E2(gp55) of Classical swine fever virus(CSFV) is the most antigenic protein being responsible for eliciting neutralizing antibodies and conferring protective immunity.
PD4抗原主要表达于靶细胞的膜上，不耐热，为分子量40kD的蛋白性抗原。
The PD4 antigen was expressed on the membrane of target cells and it was a heat-sensitive protein of40KD molecular weight.
结论通过构建基因打靶载体 ，可有目的地敲除弓形虫膜抗原基因 ，为进一步研究弓形虫侵入机制 ，探讨弓形虫病防治提供可行的方法。
These results demonstrate the utility of the gene targeting approach in the study to investigate the gene function of T. gondii. and the mechanism by which this parasite invades to the host cells.
结论通过构建基因打靶载体 ，可有目的地敲除弓形虫膜抗原基因 ，为进一步研究弓形虫侵入机制 ，探讨弓形虫病防治提供可行的方法。
These results demonstrate the utility of the gene targeting approach in the study to investigate the gene function of T. gondii. and the mechanism by which this parasite invades to the host cells.
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