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首页> 外文期刊>Journal of Immunological Methods >A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity.
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A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity.

机译:一种新型的增强型绿色荧光蛋白(EGFP)-K562流式细胞仪,用于测量自然杀伤(NK)细胞的细胞毒活性。

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摘要

Enhanced green fluorescent protein (EGFP) was stably expressed in human erythroleukaemia K562 cells (EGFP-K562) and used as target cells for measurement of natural killer (NK) cell cytotoxicity by flow cytometry. The compromised EGFP-K562 target cells were stained with propidium iodide (PI) and showed dual (green-red) fluorescent. Although the kinetic study demonstrated that the optimal incubation time for the assay was 4 h, a 2-h incubation period also gave comparable results. This new technique correlated strongly with the standard chromium (51Cr) release assay at the correlation coefficients of 0.87 and 0.89 at p-value <0.001 for 2- and 4-h incubation times, respectively. The EGFP-K562 stable cell line provides a novel method to measure NK cytotoxicity by flow cytometry without pre-staining or pre-labeling target cells.
机译:增强型绿色荧光蛋白(EGFP)在人红白血病K562细胞(EGFP-K562)中稳定表达,并用作通过流式细胞术测量自然杀伤(NK)细胞毒性的靶细胞。受损的EGFP-K562靶细胞用碘化丙啶(PI)染色,并显示双色(绿红色)荧光。尽管动力学研究表明该试验的最佳孵育时间为4 h,但2 h的孵育时间也得出了可比的结果。这项新技术与标准铬(51Cr)释放分析密切相关,在2和4小时的孵育时间下,p值<0.001的相关系数分别为0.87和0.89。 EGFP-K562稳定细胞系提供了一种通过流式细胞术测量NK细胞毒性而无需预先染色或预先标记靶细胞的新方法。

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