荧光
分子生物学
大肠杆菌
信使核糖核酸
寡核苷酸
原位
原位杂交
生物
荧光显微镜
基因
荧光原位杂交
抄写(语言学)
化学
基因表达
遗传学
物理
染色体
光学
哲学
有机化学
语言学
作者
Samuel O. Skinner,Leonardo A. Sepúlveda,Heng Xu,Ido Golding
出处
期刊:Nature Protocols
[Springer Nature]
日期:2013-05-16
卷期号:8 (6): 1100-1113
被引量:218
标识
DOI:10.1038/nprot.2013.066
摘要
We present a protocol for measuring the absolute number of mRNA molecules from a gene of interest in individual, chemically fixed Escherichia coli cells. A set of fluorescently labeled oligonucleotide probes is hybridized to the target mRNA, such that each mRNA molecule is decorated by a known number of fluorescent dyes. Cells are then imaged using fluorescence microscopy. The copy number of the target mRNA is estimated from the total intensity of fluorescent foci in the cell, rather than from counting discrete 'spots' as in other currently available protocols. Image analysis is performed using an automated algorithm. The measured mRNA copy number distribution obtained from many individual cells can be used to extract the parameters of stochastic gene activity, namely the frequency and size of transcription bursts from the gene of interest. The experimental procedure takes 2 d, with another 2-3 d typically required for image and data analysis.
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