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一种基于胸腺嘧啶核苷掺入的集落刺激因子微量测定法。

A microassay for colony-stimulating factor based on thymidine incorporation.

作者信息

Prystowsky M B, Naujokas M F, Ihle J N, Goldwasser E, Fitch F W

出版信息

Am J Pathol. 1984 Jan;114(1):149-56.

Abstract

A variety of growth factors and lectins were tested; only colony-stimulating factors CSF-1, Interleukin 3, and a T-lymphocyte GM CSF induced colony formation in semisolid medium and stimulated thymidine incorporation in liquid culture. All other growth factors and lectins were inactive in both assays. Factor-stimulated thymidine incorporation was detectable 24 hours after stimulation and reached maximal levels 4-6 days after stimulation. A convenient microassay for measuring CSF activity has been developed, enabling a large number of samples to be screened qualitatively in 2 days and permitting CSF activity to be measured quantitatively in 4-5 days. This microassay can supplement the clonal-cell assay method and be especially useful as an initial screening assay for CSF activity.

摘要

对多种生长因子和凝集素进行了测试;只有集落刺激因子CSF-1、白细胞介素3和一种T淋巴细胞GM集落刺激因子能在半固体培养基中诱导集落形成,并刺激液体培养中的胸苷掺入。所有其他生长因子和凝集素在这两种测定中均无活性。因子刺激后的胸苷掺入在刺激后24小时即可检测到,并在刺激后4 - 6天达到最高水平。已开发出一种用于测量CSF活性的便捷微量测定法,可在2天内对大量样品进行定性筛选,并能在4 - 5天内对CSF活性进行定量测定。这种微量测定法可补充克隆细胞测定法,作为CSF活性的初始筛选测定法尤其有用。

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