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猪瘟病毒E2抗原在不同酶标板上包被效果的比较
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作者 宋艳 单晶辉 +5 位作者 张茂林 段铭 关振宏 李宁 卢强 涂长春 《中国预防兽医学报》 CAS CSCD 北大核心 2011年第1期73-75,共3页
为比较杆状病毒表达的猪瘟病毒(CSFV)E2抗原在不同酶标板上的包被效果,本研究应用2μg/mL的CSFV E2分别包被Nunc Maxisorp、Cosar StripWell和JET FEP-101-896 3种酶标板,以Flyer Liquid Plate Sealer(FLPS)进行封闭,通过比较猪瘟阳性... 为比较杆状病毒表达的猪瘟病毒(CSFV)E2抗原在不同酶标板上的包被效果,本研究应用2μg/mL的CSFV E2分别包被Nunc Maxisorp、Cosar StripWell和JET FEP-101-896 3种酶标板,以Flyer Liquid Plate Sealer(FLPS)进行封闭,通过比较猪瘟阳性血清的OD450nm值,筛选包被性能最佳的酶标板。对FLPS、含10%FCS的PBST和含1%BSA的PBST的封闭效果进行比较。并比较FLPS在相同抗原条件下重复使用2次和3次对于CSFV阳性血清检测结果的影响。结果显示,在CSFV E2抗原包被的3种酶标板上,CSFV阳性血清的OD450nm值均存在显著差异(p<0.05),其中以Cosar酶标板OD450nm值最高;在Costar板上,3种封闭液间及FLPS重复使用对于CSFV阳性血清的检测结果无显著差异(p>0.05)。 展开更多
关键词 猪瘟病毒e2抗原 酶标板 包被效果
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猪瘟病毒E2蛋白抗原多肽与T4噬菌体SOC蛋白的融合表达 被引量:4
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作者 吴健敏 任兆钧 +4 位作者 余兴龙 马钢 李吉平 涂长春 张念祖 《中国兽医学报》 CAS CSCD 北大核心 2003年第1期14-17,共4页
利用 DNA重组技术将猪瘟病毒 (clascical swine fever virus,CSFV) E2蛋白主要抗原编码区基因 (m E2 )与 T4噬菌体 SOC基因融合 ,插入 T4噬菌体表达质粒 ,构建成 T4噬菌体 SOC位点表达 m E2的表达载体 p1Sm E2。将其转化至 BL2 1 (DE3 )... 利用 DNA重组技术将猪瘟病毒 (clascical swine fever virus,CSFV) E2蛋白主要抗原编码区基因 (m E2 )与 T4噬菌体 SOC基因融合 ,插入 T4噬菌体表达质粒 ,构建成 T4噬菌体 SOC位点表达 m E2的表达载体 p1Sm E2。将其转化至 BL2 1 (DE3 )菌 ,取经 IPTG诱导后表达的目的蛋白 SDC- m E2进行 SOS- PAGE、薄层凝胶扫描分析、Western blot及 EL ISA等方法检测。结果表明 ,表达的 SOC- m E2蛋白相对分子质量约 2 5 70 0 ,表达量占菌体总蛋白量的 36 .7%,并具有与 CSFV特异性抗体反应的活性。 展开更多
关键词 猪瘟病毒e2蛋白抗原多肽 T4噬菌体 SOC蛋白 融合表达
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Expression of Major Antigen Domains of E2 Gene of CSFV and Analysis of its Immunological Activity 被引量:1
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作者 Hong TIAN Xiang-tao LIU Jing-yan WU You-jun SHANG Tao JIANG Hai-xue ZHENG Qing-ge XIE 《Virologica Sinica》 SCIE CAS CSCD 2008年第4期247-254,共8页
E2 is an envelope glycoprotein of Classical swine fever virus (CSFV) and contains sequential neutralizing epitopes to induce virus-neutralizing antibodies and mount protective immunity in the natural host. In this stu... E2 is an envelope glycoprotein of Classical swine fever virus (CSFV) and contains sequential neutralizing epitopes to induce virus-neutralizing antibodies and mount protective immunity in the natural host. In this study, four antigen domains (ABCD) of the E2 gene was cloned from CSFV Shimen strain into the retroviral vector pBABE puro and expressed in eukaryotic cell (PK15) by an retroviral gene expression system, and the activity of recombinant E2 protein to induce immune responses was evaluated in rabbits. The results indicated that recombinant E2 protein can be recognized by fluorescence antibodies of CSFV and CSFV positive serum (Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China) using Western blot, indirect immunofluorescence antibody test (IFAT) and ELISA, Furthermore, anti-CSFV specific antibodies and lymphocyte proliferation were elicited and increased by recombinant protein after vaccination. In the challenge test, all of rabbits vaccinated with recombinant protein and Chinese vaccine strain (C-strain) were fully protected from a rabbit spleen virus challenge. These results indicated that a retroviral-based epitope-vaccine carrying the major antigen domains of E2 is able to induce high level of epitope-specific antibodies and exhibits similar protective capability with that induced by the C-strain, and encourages further work towards the development of a vaccine against CSFV infection. 展开更多
关键词 Classical swine fever virus (CSFV) e2 gene Antigen domains Retroviral vector Immunologicalactivity
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