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用于检测肿瘤坏死因子的无血清体外生物测定法。

Serum-free in vitro bioassay for the detection of tumor necrosis factor.

作者信息

Kramer S M, Carver M E

出版信息

J Immunol Methods. 1986 Nov 6;93(2):201-6. doi: 10.1016/0022-1759(86)90189-4.

Abstract

A sensitive, reproducible in vitro bioassay is described for quantitating the cytolytic activity of tumor necrosis factor (TNF). The assay target cells, murine connective tissue L-M, are propagated and the assay performed under serum-free conditions. The quantitation of cytolytic activity is based on the ability of TNF to lyse L-M cells in the presence of actinomycin D, as measured by crystal violet dye uptake of residual viable cells. The assay is sensitive to 88 pg/ml TNF-alpha. The simplicity of the culture medium combined with high sensitivity and low variability make this a particularly well-suited bioassay for routine detection of TNF cytolytic activity.

摘要

本文描述了一种灵敏、可重复的体外生物测定法,用于定量肿瘤坏死因子(TNF)的细胞溶解活性。测定的靶细胞为小鼠结缔组织L-M细胞,在无血清条件下进行增殖和测定。细胞溶解活性的定量基于TNF在放线菌素D存在下裂解L-M细胞的能力,通过残留活细胞对结晶紫染料的摄取来测量。该测定法对88 pg/ml的TNF-α敏感。培养基的简单性、高灵敏度和低变异性使其成为常规检测TNF细胞溶解活性的特别合适的生物测定法。

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