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机构地区:[1]湖南医科大学肿瘤研究所
出 处:《中国病理生理杂志》1991年第6期646-649,共4页Chinese Journal of Pathophysiology
基 金:国家自然科学基金
摘 要:本文用~3H-TdR和BudR同时掺入体外培养细胞并先后以免疫化学和放射自显影方法显示DNA合成期标记的细胞。结果表明,BudR免疫化学法显示的S期标记细胞与~3H-TdR放射自显影法标记的结果高度吻合,进一步证明具有独特的优点,可以取代经典的同位素法进行细胞动力学研究。同时,本文还对贴壁细胞和悬浮培养细胞的BudR掺入条件作了初步探讨。Hela cells and human peripheral lymphocells were labeled with tritiated thymidine (~3H-TdR) and 5-bromodeoxyuridine (BudR) simultaneously for 1-12 hours. The S phase (DNA synthesis) cells were then detected by monoclonal antibody against BudR (BU-1) through immunocytochemistry and autoradiography, respectively. The labeling indexes of BUdR and ~3H-TdR in the same sample were almost the same. This nonisotopic technique offers a faster and relatively simplar alternative method for determing labeling indexes of human tumors.
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