质量细胞仪
流式细胞术
多路复用
单细胞分析
微流控
计算生物学
蛋白质组学
细胞
荧光显微镜
定量蛋白质组学
细胞仪
细胞生物学
纳米技术
生物
荧光
化学
计算机科学
材料科学
分子生物学
物理
生物化学
电信
量子力学
基因
表型
作者
Lü Huang,Sean A. Michael,Yangfan Chen,Hongkai Wu
标识
DOI:10.1002/asia.201700404
摘要
Abstract Single‐cell measurements have played a critical role in revealing the complex signaling dynamics and heterogeneity present in cells, but there is still much to learn. Measuring samples from bulk populations of cells often masks the information and dynamics present in subsets of cells. Common single‐cell protein studies rely on fluorescent microscopy and flow cytometry but are limited in multiplexing ability owing to spectral overlap. Recently, technology advancements in single‐cell proteomics have allowed highly multiplexed measurement of multiple parameters simultaneously by using barcoded microfluidic enzyme‐linked immunosorbent assays and mass cytometry techniques. In this review, we will describe recent work around multiparameter single‐cell protein measurements and critically analyze the techniques.
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