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一种源自畸胎癌的细胞系TerC上的H-2表达。

H-2 expression on a teratocarcinoma-derived cell line, TerC.

作者信息

Searls D B, Edidin M

出版信息

J Natl Cancer Inst. 1982 Dec;69(6):1311-5.

PMID:6958907
Abstract

The murine teratocarcinoma-derived cell line TerC, previously thought to lack products of the major histocompatibility locus H-2, was shown to express low levels of K- and D-end H-2 specificities with the use of a sensitive cytotoxic assay. The assay, based on the ability of antibody and complement to inhibit uptake of the thymidine analogue [125I]5-iodo-2'-deoxyuridine, detected appropriate public and private specificities, as demonstrated with the use of oligospecific antisera and by absorption analyses. A series of clone of TerC varied only slightly in H-2 expression, and there was no tendency for expression to increase with time in culture; thus the low levels of H-2 were not the result of a differentiating subpopulation.

摘要

鼠畸胎瘤衍生细胞系TerC,以前被认为缺乏主要组织相容性位点H-2的产物,通过一种灵敏的细胞毒性测定法显示其表达低水平的K和D端H-2特异性。该测定法基于抗体和补体抑制胸苷类似物[125I]5-碘-2'-脱氧尿苷摄取的能力,检测到了合适的公共和私有特异性,这通过使用寡特异性抗血清和吸收分析得以证明。TerC的一系列克隆在H-2表达上仅有轻微差异,且在培养过程中表达没有随时间增加的趋势;因此,低水平的H-2并非分化亚群的结果。

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