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抗DNA-8-甲氧基补骨脂素光加合物免疫血清。

Immune serum against anti-DNA-8-methoxypsoralen photoadduct.

作者信息

Zarebska Z, Jarzabek-Chorzelska M, Chorzelski T, Jabłońska S

出版信息

Z Naturforsch C Biosci. 1984 Jan-Feb;39(1-2):136-40. doi: 10.1515/znc-1984-1-222.

Abstract

Specific immune serum against photo-damaged DNA with the photoadducts of 8-methoxypsoralen (8-MOP) was obtained. The antigenic determinant is a polynucleotide chain with a mono-photoadduct: a coumarin moiety of psoralen linked through a cyclobutane ring to the 5,6-bond of thymine. The specific rabbit antiserum was used in the immunofluorescence method, for the detection of photodamaged DNA in the kinetoplasts and nuclei of unicellular organisms Crithidia luciliae, in the nuclei of snap-frozen tissue of mammals, and in human blood lymphocytes. Detection by the immunofluorescence method was limited by psoralen availability in situ; the psoralen concentration should be in the range 0.05-0.2 microgram/cm2 on specimens submitted to a topical application or about 1 microgram/ml in cell suspension. The long-wave ultraviolet light (UV-A) exposure dose applied to the nuclei should exceed 1 J/cm2.

摘要

获得了针对具有8-甲氧基补骨脂素(8-MOP)光加合物的光损伤DNA的特异性免疫血清。抗原决定簇是具有单光加合物的多核苷酸链:补骨脂素的香豆素部分通过环丁烷环与胸腺嘧啶的5,6-键相连。使用特异性兔抗血清通过免疫荧光法检测单细胞生物鲁氏锥虫的动基体和细胞核、哺乳动物速冻组织的细胞核以及人血淋巴细胞中的光损伤DNA。免疫荧光法检测受原位补骨脂素可用性的限制;对于局部应用的标本,补骨脂素浓度应在0.05-0.2微克/平方厘米范围内,或在细胞悬液中约为1微克/毫升。施加到细胞核的长波紫外线(UV-A)暴露剂量应超过1焦耳/平方厘米。

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