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用[3H]胸腺嘧啶核苷和[125I]碘脱氧尿苷进行双重标记作为一种在体内确定注射的DNA和细胞命运的方法。

Double labeling with [3H]thymidine and [125I]iododeoxyuridine as a method for determining the fate of injected DNA and cells in vivo.

作者信息

Myers D K, Feinendegen L E

出版信息

J Cell Biol. 1975 Nov;67(2PT.1):484-8. doi: 10.1083/jcb.67.2.484.

Abstract

Mice were injected intravenously and intraperitoneally with preparations of intestinal nucleoprotein, spleen nuclei, mouse thymus cells, or human kidney T cells whose DNA had been labeled with both [3H]thymidine (TdR) and [125I]-iododeoxyuridine (IUdR). Since free TdR is reutilized more efficiently than free IUdR produced by enzymic hydrolysis of the exogenous DNA, the ratio of [3H]TdR/[125I]IUdR in the DNA fraction of the tissues of the recipient mice provides a measure of the amount of intact exogenous DNA in the tissue. In most instances, the doubly labeled exogenous DNA was almost completely hydrolyzed within 1 day injection, but survival of the DNA from whole cells could be demonstrated in some cases.

摘要

给小鼠静脉内和腹腔内注射经[3H]胸腺嘧啶核苷(TdR)和[125I] - 碘脱氧尿苷(IUdR)标记DNA的肠核蛋白制剂、脾细胞核、小鼠胸腺细胞或人肾T细胞。由于游离TdR比外源性DNA酶解产生的游离IUdR更有效地被再利用,受体小鼠组织DNA部分中[3H]TdR/[125I]IUdR的比值可衡量组织中完整外源性DNA的量。在大多数情况下,双标记的外源性DNA在注射后1天内几乎完全水解,但在某些情况下可证明全细胞DNA的存活。

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DNA turnover and thymidine re-utilization in mouse tissues.小鼠组织中的DNA周转与胸苷再利用
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