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作 者:周德南[1] 甘友全[1] 吴英德[1] 宋向群[1] 杨克政[1] 黄秉琰[1]
机构地区:[1]广西肿瘤防治研究所
出 处:《广西医科大学学报》1996年第4期7-9,共3页Journal of Guangxi Medical University
基 金:广西区科委资助
摘 要:用亲和层析法提纯马抗AFP,采用氯胺T改良法标记125I,经SephadexG50柱分离,以r计数与紫外同步监测进行标记物的收集。并对125I-抗AFP制备方法及其稳定性等进行探讨和测定。结果:125I和抗AFP的利用率分别为60%~80%和50%~73%;标记率为65%~83%,125I-抗AFP的比放射性为55.5~74MBq/mg;放化纯度5d内为97%~98%,14d为93%;抗体活性标记后与标记前基本不变,4℃保存5d和14d均无降低。表明125I-抗AFP的生物活性及稳定性良好。AFP antibody (Ab AFP) from horse serum was purified by affinity chromatography, 125 I was marked by improved P toluene sulphonamide method,and the marker was collected by r counter and ultrariolet way after it was separated by sephadex G 50 The method of preparation and the stablity of 125 I Ab AFP were examined Result:Utilixation rate of 125 I and Ab AFP was 60% ̄80% and 50% ̄73% respectively Marker rate:65% ̄83%; 125 I Ab AFP's specific radioactivity:55 5 ̄74MBq/mg;radiochemical purity:97% ̄98%(five days) and 93%(fourteen days) The activity of the antibody after marking was very similar to that before marking,and did not decrease after preservation for five days or fourteen days at 4℃ The result shows that the biologic activity and stablity of 125 I Ab AFP are good
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