This section describes different methods of analyzing cells after transfection, such as flow cytometry, fluorometry, laser-scanning molecular imaging, luminometry, real-time qPCR, microscopy, spectrometry, and western blot analysis. It also provides guidelines and methods that you can use for the analysis of transfected cells. The methods can be used to determine transfection efficiencies and to perform more in-depth analyses of the expression of your favorite gene/protein. However, depending on your cells, reagents, or equipment availability these methods should be modified to fit your laboratory needs.
Related Topics: Transfection, Instrument-Based Transfection Methods, and Chemical- and Viral-Based Transfection.
There are many factors that can influence transfection efficiency, a number of which are specific to the target cell. Cell-related factors affecting transfection include cell density, cell size, replication state, passage number, health of cells, biomolecule type, and concentration. Some factors are method specific; for example, electroporation parameters such as voltage, capacitance, and resistance strongly affect transfection efficiency. Therefore, to obtain high efficiencies, all relevant factors should be considered when planning transfection experiments.
Frequently, after any transfection experiment, it is important to assess the efficiency of transfection and the impact of transfection on the cells. Analysis of transfection efficiency can be as simple as confirming the expression of your gene of interest. However, in many cases assessment of transfection involves determining the total expression level of your gene of interest, determining the number of positive cells within a transfected population (% positive cells), and/or visual confirmation of your protein of interest (Jordan et al. 2007).
Most methods for measuring protein expression level of your transfected cell will determine the total expression from a population of transfected cells. Measurement of total gene expression can be done through real-time quantitative PCR (real-time qPCR), western blot analysis, molecular imaging, and fluorometry. Determining the number of positive cells within a transfected cell population can be performed by microscopy and flow cytometry. Finally, confirming localization of your protein of interest can be done by microscopy.
Reporter genes, such as green fluorescent protein (GFP), luciferase, or β-galactosidase can be used to analyze transfection efficiency because their expression can be easily monitored. They can also be used to standardize transfection efficiencies between different transfection experiments by comparing the expression levels of their products. Reporter genes can be used alone or fused to a gene of interest to determine the protein expression level, the number of positive cells, or the location of the protein being studied.
Following are some of the most common methods used for posttransfection analysis.
A flow cytometer can determine the number of positive cells within a transfected cell population (% positive cells). In addition, a flow cytometer with sorting abilities can enrich for positive cell populations. However, flow cytometry requires that the cells either express a fluorescent protein, such as GFP, or your protein of interest must be labeled with a fluorescent molecule.
For more information about flow cytometry, visit http://flowcyt.sourceforge.net/.
Requirements or Limitations
A fluorometer can detect a wide range of fluorescence. Extracts from cells expressing fluorescent protein can be used to measure the expression level of your gene in the transfected cells.
For more information about fluorescent protein detection in cell extracts, see Wilson J and Segal A (1998). Measuring intracellular enhanced green fluorescent protein with the VersaFluor™ fluorometer. Bio-Rad bulletin 2368.
Laser-scanning molecular imagers can detect a wide range of fluorescence. With the use of appropriate fluorophores, western blots or gels can be quantitatively analyzed with a scanner. In addition to analyzing western blots or gels, scanners can also directly detect and quantify lysate from a population of cells expressing a fluorescent protein, such as GFP. The ability to detect fluorescence allows the scanner to directly analyze cell lysate without running a gel.
For more information about laser-scanning molecular imaging, see Bio-Rad bulletin 2752. Applications for Molecular Imager FX Systems: Instrument settings.
A luminometer is an instrument that measures light intensity. Expression or co-expression of luciferase, which emits light after interacting with its substrate, can be used for quantitative analysis of total protein expression.
For more information about luminometry and luciferase assays, see Sambrook J and Russell D (2001). Analysis of gene expression in cultured mammalian cells. In Molecular Cloning: A laboratory manual, Third Ed. (Woodbury, NY: Cold Spring Harbor Laboratory Press), 17.96.
Microscopy allows direct visualization of transfected cells. Microscopy can be used to count the number of transfected cells for estimation of positive cell numbers. Microscopy can also be used to confirm the correct localization of your protein of interest. Visualization of cells transfected with your gene of interest can be accomplished in several ways. Expression or co-expression of a fluorescent protein, such as GFP, will allow the direct identification of your transfected cells. However, a non-fluorescent protein must be labeled for visualization. Immunofluorescence, chemical labeling, and immunohistochemistry techniques can be used to label proteins. In general, microscopy cannot be used for quantitative measurement of transfection efficiency unless you have image analysis software that can count and quantitate positively transfected cells.
For more information about chemical and immunofluorescent labeling, fluorescence microscopy, and immunohistochemistry techniques, visit:
Real-time qPCR can quantify the expression level of a transgene or measure the degree to which a gene silencing (knockdown) experiment has been effective. It is fast and, because it requires little starting material, it is applicable when transfected cells are available in limited amounts.
Using real-time qPCR, one can determine the relative abundance of specific messenger RNA (mRNA) compared to a control. Additionally, real-time qPCR can be used to assess how the knockdown of one gene may affect the expression of other genes in the pathway. However, it does not directly measure or identify the presence of protein. Therefore, any problems post-mRNA synthesis, such as problems during protein translation, will not be identified with this method. As a result, you may observe mRNA production where there may not be any protein synthesis.
A spectrophotometer is an instrument that measures light intensity as a function of color or wavelength. In fact, β-galactosidase assays can be used to determine transfection efficiency by measuring colorimetric changes associated with β-galactosidase activity.
For more information about spectrophotometry and β-galactosidase assays, see:
Western blot analysis can be used to identify or quantitate the total expression of your transfected gene from a population of cells. With western blot analysis, you can determine the relative expression level of your transfected protein in a population of cells. This method of quantitation requires the use of an internal control, such as GAPDH or β-actin.
For more information about western blot analysis, see:
Jordan E et al. (2007). Optimization of electroporation conditions with the Gene Pulser MXcell™ electroporation system. Bio-Rad bulletin 5622.
Nickoloff JA, ed. (1995). Animal Cell Electroporation and Electrofusion Protocols (Methods in Molecular Biology, volume 48) (Totowa, NJ: Humana Press Inc.).
SourceForge, Inc. (2007). Bioinformatics Standards for Flow Cytometry. http://flowcyt.sourceforge.net/, accessed August 4, 2009.
Wilson J and Segal A (1998). Measuring intracellular enhanced green fluorescent protein with the VersaFluor™ fluorometer. Bio-Rad bulletin 2368.
Laser-Scanning Molecular Imaging
Bio-Rad bulletin 2752. Applications for Molecular Imager FX systems: Instrument settings.
Sambrook J and Russell D (2001). Analysis of gene expression in cultured mammalian cells. In Molecular Cloning: A Laboratory Manual, 3rd ed. (Woodbury, NY: Cold Spring Harbor Laboratory Press), 17.96.
MC Services. Fluorescence Imaging. http://www.mwrn.com/microscopy/light/fluorescence.aspx, accessed August 4, 2009.
Rogers S. Cell Biology Applications of Fluorescence Microscopy. IHC World, LLC. http://www.ihcworld.com/_protocols/immunofluorescence/immunofluorescence.htm, accessed August 4, 2009.
Real-Time Quantitative PCR
Bio-Rad Bulletin 5279. Real-time PCR applications guide.
Nielsen DA et al. (1983). Expression of a preproinsulin-beta-galactosidase gene fusion in mammalian cells. Proc Natl Acad Sci USA 80, 5198–5202. Protocol Online. B-Gal Staining of Eukaryotic Cells in Vitro. http://www.protocol-online.org/cgi-bin/prot/view_cache.cgi?ID=1240, accessed August 4, 2009.
Sambrook J, Fritsch EF, Maniatis T, eds. (1989). Molecular Cloning: A Laboratory Manual, 2nd ed. (Woodbury, NY: Cold Spring Harbor Laboratory Press).
Western Blot Analysis
Bio-Rad bulletin 5723. Increase western blot throughput with multiplex fluorescent detection. westernblotting.org. http://www.westernblotting.org/, accessed August 4, 2009.
Call us at 1-800-268-0213
Please reenter your email address in the correct format.
Please enter your email address.
Your subscription information already exists, we will send you an email with specific instructions to manage your existing subscription profile.
To receive the latest news, promotions, and more, sign up for Bio-Rad updates by entering your email address below. You can elect to receive only the types of Bio-Rad communications that are of interest to you..
Copyright © 2017 Bio-Rad Laboratories, Inc. All rights reserved.