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Fluorescence Produced by Transfection Reagents Can Be Confused with Green Fluorescent Proteins in Mammalian Cells
Author(s) -
Baoqing Guo,
Andrew Pearce,
K.E.A. Traulsen,
Anne C. Rintala,
H. Lee
Publication year - 2001
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/01312st02
Subject(s) - green fluorescent protein , aequorea victoria , transfection , fluorescence , fluorescence microscope , fusion protein , microbiology and biotechnology , biology , flow cytometry , reporter gene , chemistry , gene expression , recombinant dna , gene , biochemistry , physics , quantum mechanics
The Aequorea victoria green fluorescent protein (GFP) reporter system is a convenient way to monitor gene expression and other cellular functions in mammalian cells. To study gene expression, a GFP-fusion plasmid construct is often transfected into mammalian cells using a variety of methods including calcium phosphate- and liposome-based DNA transfer. Subsequently, the expression of GFP-fusion protein is monitored by fluorescence microscopy or flow cytometry. Here, we report that certain transfection reagents can produce fluorescence that can be detected in a wide range of wavelengths, which can be confused with GFP-fusion protein. The fluorescence false positives can be a problem, particularly when the GFP expression levels are low. To improve the GFP-based detection or screening methods, it is imperative to include an appropriate negative control and to detect GFP using a narrow-wavelength emission filter corresponding to the emission spectrum around the GFP peak.

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