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本文引用的文献

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Brilliant violet fluorophores: a new class of ultrabright fluorescent compounds for immunofluorescence experiments.绚丽的紫色荧光团:一类用于免疫荧光实验的新型超亮荧光化合物。
Cytometry A. 2012 Jun;81(6):456-66. doi: 10.1002/cyto.a.22043. Epub 2012 Apr 6.
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Detection of circulating platelet-monocyte complexes in persons infected with human immunodeficiency virus type-1.检测感染人类免疫缺陷病毒 1 型的个体中的循环血小板-单核细胞复合物。
J Virol Methods. 2012 May;181(2):170-6. doi: 10.1016/j.jviromet.2012.02.005. Epub 2012 Feb 23.
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Analysis of apoptosis methods recently used in Cancer Research and Cell Death & Disease publications.对癌症研究以及《细胞死亡与疾病》出版物中最近使用的细胞凋亡方法的分析。
Cell Death Dis. 2012 Feb 2;3(2):e263. doi: 10.1038/cddis.2012.2.
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Mammalian cells as biopharmaceutical production hosts in the age of omics.在组学时代,哺乳动物细胞作为生物制药生产的宿主。
Biotechnol J. 2012 Jan;7(1):75-89. doi: 10.1002/biot.201100369. Epub 2011 Dec 16.
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Antibody colocalization microarray: a scalable technology for multiplex protein analysis in complex samples.抗体共定位微阵列:一种用于复杂样本中多重蛋白质分析的可扩展技术。
Mol Cell Proteomics. 2012 Apr;11(4):M111.011460. doi: 10.1074/mcp.M111.011460. Epub 2011 Dec 14.
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Getting the whole picture: combining throughput with content in microscopy.纵观全局:将通量与显微镜中的内容相结合。
J Cell Sci. 2011 Nov 15;124(Pt 22):3743-51. doi: 10.1242/jcs.087486.
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Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry.使用成像细胞术对神经母细胞瘤单细胞中微小RNA及其靶基因的表达进行可视化和定量分析。
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A regression model approach to enable cell morphology correction in high-throughput flow cytometry.一种用于在高通量流式细胞术中实现细胞形态校正的回归模型方法。
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Intercellular communication by exchange of cytoplasmic material via tunneling nano-tube like structures in primary human renal epithelial cells.原发性人肾上皮细胞通过形成类似隧道纳米管的结构进行细胞质物质交换实现细胞间通讯。
PLoS One. 2011;6(6):e21283. doi: 10.1371/journal.pone.0021283. Epub 2011 Jun 27.
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Laser scanning cytometry and its applications: a pioneering technology in the field of quantitative imaging cytometry.激光扫描细胞术及其应用:定量成像细胞术领域的一项开创性技术。
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成像流式细胞术:应对生物系统中的异质性。

Imaging flow cytometry: coping with heterogeneity in biological systems.

机构信息

Immune Disease Institute and Program in Cellular and Molecular Medicine, Children's Hospital Boston and Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Histochem Cytochem. 2012 Oct;60(10):723-33. doi: 10.1369/0022155412453052. Epub 2012 Jun 27.

DOI:10.1369/0022155412453052
PMID:22740345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3524563/
Abstract

Imaging flow cytometry (IFC) platforms combine features of flow cytometry and fluorescent microscopy with advances in data-processing algorithms. IFC allows multiparametric fluorescent and morphological analysis of thousands of cellular events and has the unique capability of identifying collected events by their real images. IFC allows the analysis of heterogeneous cell populations, where one of the cellular components has low expression (<0.03%) and can be described by Poisson distribution. With the help of IFC, one can address a critical question of statistical analysis of subcellular distribution of proteins in a cell. Here the authors review advantages of IFC in comparison with more traditional technologies, such as Western blotting and flow cytometry (FC), as well as new high-throughput fluorescent microscopy (HTFM), and discuss further developments of this novel analytical technique.

摘要

成像流式细胞术(IFC)平台结合了流式细胞术和荧光显微镜的特点,并结合了数据处理算法的进步。IFC 允许对数千个细胞事件进行多参数荧光和形态分析,并且具有通过其真实图像识别已采集事件的独特功能。IFC 允许对异质细胞群体进行分析,其中一个细胞成分的表达水平较低(<0.03%),并且可以用泊松分布来描述。借助 IFC,可以解决细胞内蛋白质亚细胞分布的统计分析中的一个关键问题。在这里,作者综述了 IFC 相对于更传统的技术(例如 Western blot 和流式细胞术(FC))以及新型高通量荧光显微镜(HTFM)的优势,并讨论了该新型分析技术的进一步发展。