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纳克量DNA中二胸腺嘧啶环丁烷二聚体的免疫测定。

Immunoassay of dithymidine cyclobutane dimers in nanogram quantities of DNA.

作者信息

Strickland P T, Creasey J S

机构信息

Department of Environmental Health Sciences, Johns Hopkins University School of Hygiene and Public Health, Baltimore, MD.

出版信息

IARC Sci Publ. 1988(89):341-4.

PMID:3198218
Abstract

Immunological assays for DNA photoproducts, which have been in use for a number of years, provide a rapid means for quantifying photodamage in DNA. Radioimmunoassays (RIA) are capable of measuring photoproducts in microgram quantities (1-10 micrograms) of DNA extracted from biological samples, e.g., animal skin or cultured cells. We have refined an indirect enzyme-linked immunosorbent assay (ELISA) for the analysis of cyclobutadithymidine (T-T) photoproducts in nanogram quantities (3-100 ng) of DNA. T-T photoproducts were detectable in 30 ng DNA irradiated with a minimum of 10 J/m2 of 254 nm ultraviolet light (UV). The efficiency of T-T induction in DNA was approximately 4000-fold lower per unit dose using a solar-simulating UV radiation source (290-400 nm) than with 254 nm radiation. The assay was used to measure T-T photoproducts induced by solar-simulated UV radiation in hamster skin and human skin and should be useful for the routine analysis of photoproducts in small amounts of DNA (500-1000 ng) available from human skin biopsies.

摘要

用于DNA光产物的免疫测定法已经使用多年,它为定量DNA中的光损伤提供了一种快速方法。放射免疫测定法(RIA)能够测量从生物样品(如动物皮肤或培养细胞)中提取的微克量(1-10微克)DNA中的光产物。我们改进了一种间接酶联免疫吸附测定法(ELISA),用于分析纳克量(3-100纳克)DNA中的环丁烷二聚胸苷(T-T)光产物。在用至少10 J/m2的254纳米紫外线(UV)照射的30纳克DNA中可检测到T-T光产物。使用模拟太阳紫外线辐射源(290-400纳米)时,DNA中T-T诱导效率比254纳米辐射时每单位剂量低约4000倍。该测定法用于测量模拟太阳紫外线辐射在仓鼠皮肤和人皮肤中诱导的T-T光产物,应该有助于对从人皮肤活检获得的少量DNA(500-1000纳克)中的光产物进行常规分析。

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