Cited by 476Advanced Proteomics Techniques and ApplicationsMolecular Biology Techniques and ApplicationsAdvanced Biosensing Techniques and Applications

The use of total protein stains as loading controls: an alternative to high-abundance single-protein controls in semi-quantitative immunoblotting

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Aldridge, Georgina M., Podrebarac, David M., Greenough, William T., Weiler, Ivan Jeanne·2008·Journal of Neuroscience Methods

Abstract

Western blots are used to estimate the relative concentrations of proteins of interest based on staining by specific antibodies. Quantitative measurements are often subject to error due to overloading of the loading control and over-reliance on normalization. We have found that at the protein concentrations normally used to quantify most low-abundance proteins of interest, frequently used single-protein loading controls, such as glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and beta-actin, do not accurately reflect differences in protein concentration. Two total protein stains, SYPRO Ruby and Amido Black, were compared and found to be acceptable alternatives to single-protein controls. Although we cannot prove that high-abundance loading controls are inaccurate under all possible conditions, we conclude that the burden of proof should lie with the researcher to demonstrate that their loading control is reflective of quantitative differences in protein concentration.

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Crossref · 10.1016/j.jneumeth.2008.05.003

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  • Total protein provides a stable reference measure that accounts for variation in protein loading and in the amount of protein transferred to the membrane, and can have superior linearity over a range of concentrations when compared to using a single reference protein.

    “Total protein provides a stable reference measure that accounts for variation in protein loading and in the amount of protein transferred to the membrane (Welinder and Ekblad, 2011), and can have superior linearity over a range of concentrations when compared to using a single reference protein (Aldridge et al., 2008; Eaton et al., 2013).”

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References 11 · Cited by 476

Authors
Aldridge, G. M., Podrebarac, D. M., Greenough, W. T., & Weiler, I. J.
Affiliations
University of Illinois Urbana-Champaign (US)
Corresponding author
Aldridge, Georgina M.
Venue
Journal of Neuroscience Methods
Publisher
Elsevier BV
Published
2008-07
Volume
172
Issue
2
Pages
250-254
ISSN
0165-0270 (ISSN-L)
OpenAlex
W2079516818
Cited by
476
References
11
Citations by year
2026: 18 · 2025: 16 · 2024: 24 · 2023: 17 · 2022: 27 · 2021: 34 · 2020: 41 · 2019: 30 · 2018: 33 · 2017: 33 · 2016: 23 · 2015: 39 · 2014: 39 · 2013: 33 · 2012: 31
FWCI
5.34
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience Methods (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute of Mental Health (MH-35321, R01MH035321, R37MH035321)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD007333, T32HD007333)
Topics
  • Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Molecular Biology Techniques and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced Biosensing Techniques and Applications
Keywords
loading control, SYPRO Ruby, amido black, glyceraldehyde-3-phosphate dehydrogenase, beta-actin, protein quantification, normalization, overloading, low-abundance proteins
MeSH terms
Disks Large Homolog 4 Protein, Amido Black, Amino Acid Sequence, Animals, Brain Chemistry, Coloring Agents, Membrane Proteins, Nerve Tissue Proteins, Neurochemistry, Organometallic Compounds, Staining and Labeling, Subcellular Fractions, Blotting, Western, Proteomics, Intracellular Signaling Peptides and Proteins, Mitogen-Activated Protein Kinase 3, Mice, Guanylate Kinases

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