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一种改进的细胞增殖实验中相对响应计算技术。

An improved technique for calculating relative response in cellular proliferation experiments.

出版信息

Cytometry A. 2010 Oct;77(10):909-10. doi: 10.1002/cyto.a.20935.

Abstract

Investigating the response of cells to specific agonists may involve the use of cell tracking dyes to assess the extent of stimulated proliferation, frequently reported as the proliferation index (PI). Calculation of PI uses a model for cell division that expects the cell number to double as cells proliferate through each successive generation. It is often useful to compare the PI of a stimulated control population with that of a population in the presence of some agent, whether chemical, pharmacologic, or cellular. For such comparison studies, the nature of the metric being used must be taken into account to accurately assess the extent of inhibition. Specifically, the metric used in ModFit LT (Verity Software House, Topsham, ME) and in FCS Express (De Novo Software, Los Angeles, CA) uses a metric with a lower limit of unity, whereas the metric used in FlowJo (Treestar, Ashland, OR) has a lower limit of zero. For studies involving cell proliferation comparisons using tracking dye dilution, a new equation is proposed as the appropriate calculation to use when determining the percent of relative response based on proliferation index values for a metric whose lower limit is unity.

摘要

研究细胞对特定激动剂的反应可能需要使用细胞跟踪染料来评估受刺激增殖的程度,通常以增殖指数 (PI) 来表示。PI 的计算使用了一种细胞分裂模型,该模型预计细胞数量会随着细胞在每个连续代中增殖而翻倍。比较刺激对照群体的 PI 与存在某种试剂(无论是化学试剂、药理学试剂还是细胞)的群体的 PI 通常很有用。对于此类比较研究,必须考虑所使用的度量标准的性质,以准确评估抑制的程度。具体而言,在 ModFit LT(Verity Software House,Topsham,ME)和 FCS Express(De Novo Software,洛杉矶,CA)中使用的度量标准具有下限为 1,而在 FlowJo(Treestar,阿什兰,OR)中使用的度量标准具有下限为 0。对于涉及使用跟踪染料稀释的细胞增殖比较的研究,当根据增殖指数值确定基于增殖指数值的相对反应的百分比时,建议使用一个新的方程,该方程适用于下限为 1 的度量标准。

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