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作 者:宋永继[1] 侯俊[2] 徐军[1] 刘爱霞[1] 刘佳[1] 赵静[1] 郭静霞[1] 李靖 闫静肖 李伯安[1] 毛远丽[1]
机构地区:[1]中国人民解放军第三〇二医院临检中心,北京100039 [2]中国人民解放军第三〇二医院实验技术保障中心,北京100039 [3]北京热景生物技术有限公司
出 处:《中华实验和临床病毒学杂志》2013年第2期129-131,共3页Chinese Journal of Experimental and Clinical Virology
基 金:首都医学发展基金重点项目(2005-2038);首都临床特色应用研究(Z111107058811068)
摘 要:目的利用小扁豆凝集素(LCA)建立基于微量离心柱的甲胎蛋白异质体L3(AFP—L3)的纯化方法。方法采用硫酸铵分级沉淀的方法由小扁豆中提取凝集素,偶联到活化的琼脂糖凝胶4B(sephrose4B)上,灌注离心柱,制备AFP—L3亲和吸附离心管。血清加入离心管后经吸附和洗脱,便可获得纯化的AFP—L3。随机选取10例AFP阳性患者血清,应用亲和吸附纯化法纯化AFP.L3后应用电化学发光法检测,并与传统的亲和免疫电泳方法相比较。结果10例患者血清经纯化后,AFP-L3检测结果有8例〉5ng/ml,亲和免疫电泳有6例呈现阳性反应。结论成功建立基于微量离心柱的亲和吸附纯化AFP—L3的方法,该方法具有较高的灵敏度,重复性好并且操作简便更利于临床实验室应用。Objective To establish a purificatory method of alpha-fetoprotein variant (AFP-L3) based on microspincolumn with lens culinaris agglutinin (LCA). Methods LCA was isolated by ammonium sulfate precipitation method from lens culinaris. AFP-L3 affinity adsorption microspincolumns which were made from LCA coupled with activated Sepharose 4B were prepared. By adding into the centrifuge column, serum was absorbed and eluted to purify AFP-L3. The results of purified AFP-L3 detection of 10 cases AFP positive sera by electro-chemiluminescence immunoassay were compared with traditional crossed affinity immunoelectropboresis. Results 8 of 10 eases AFP-L3 concentration were greater than 5 ng/ml in purified sera. Six cases show positive reaction in affinity immune cross electrophoresis experiment. Conclusion Successfully established purification method of AFP-L3 by affinity absorption based on microspincolumn. The method was more conducive to clinical laboratory applications due to its high sensitive and easy operation.
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