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作 者:许伟群[1] 朱苹[1] 苏东辉[1] 黄爱明[1] 刘梁英[1]
机构地区:[1]福建医科大学微生物学教研室
出 处:《中国人兽共患病杂志》1999年第1期47-49,共3页Chinese Journal of Zoonoses
摘 要:由于细菌脂多糖(LPS)水溶性差,用传统的ELISA检测抗-LPS抗体抗原用量大,敏感性不理想。我们用能和LPS结合的多粘菌素B(PMB)预先包被微量反应板,可使随后加入的LPS(光滑型和粗糙型)包被效率增加,检测抗-LPS抗体(单克隆抗体和动物免疫血清)的敏感性显著增加(最高达128倍)。Conventional ELISA for anti lipopolysaccharide(LPS)antibodies is not ideally sensitive because of the poor solubility of bacterial LPS.A new ELISA by precoating the microtiter plates with ploymyxin B was developed,a cyclic antibiotic that is able to bind with LPS,to improve the coating efficiency of LPS.In comparison with the conventional ELISA /in which LPS was directly coated onto the plates,the new method detected much higher(128-fold as the highest)anti LPS titers in murine antisera and monoclonal antibody raised against Re LPS.
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