Freezing diluted bovine serum albumin standards does not significantly affect standard curves

Total protein isolation followed by quantitation using a colorimetric method, such as the bicinchoninic acid (BCA) assay is a common laboratory protocol. Protein concentrations are determined by comparing extracted samples to a standard curve generated from serial dilutions of a reference protein, such as bovine serum albumin (BSA). This study aimed to identify the most reproducible and accurate method for quantifying protein concentrations in an experimental series over time. We analyzed the effect of serial freeze-thaws, inter-person and intra-person variability in standard preparation and assay execution. Absorbance was measured at 565 nanometers (nm) using an Epoch Microplate Spectrophotometer (Agilent Technologies, Inc., Santa Clara, CA) with Gen5 Data Analysis software. The most consistent and accurate method for determining the protein concentrations over time is to prepare a large batch of diluted BSA standards, aliquot them into small portions, and store them frozen.

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Publication Details

Journal
BioTechniques
Published
2025-03-04
DOI
https://doi.org/10.1080/07366205.2025.2502268
Citations
1
Primary Topic
Clinical Laboratory Practices and Quality Control
Type
article
Field-Weighted Citation Impact
1.16

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article

Freezing diluted bovine serum albumin standards does not significantly affect standard curves

Rachelle Sheets, Adrienne C. Scheck, Phillip Stafford, Theresa Currier Thomas et al.
1 citations
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Clinical Laboratory Practices and Quality Control
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article

Freezing diluted bovine serum albumin standards does not significantly affect standard curves

Rachelle Sheets, Adrienne C. Scheck, Phillip Stafford, Theresa Currier Thomas, Bhavik Rajaboina, Mitchell L. Haddock, Liam Curtin, Caitlin E. Bromberg
article en
1 citations

Abstract

Total protein isolation followed by quantitation using a colorimetric method, such as the bicinchoninic acid (BCA) assay is a common laboratory protocol. Protein concentrations are determined by comparing extracted samples to a standard curve generated from serial dilutions of a reference protein, such as bovine serum albumin (BSA). This study aimed to identify the most reproducible and accurate method for quantifying protein concentrations in an experimental series over time. We analyzed the effect of serial freeze-thaws, inter-person and intra-person variability in standard preparation and assay execution. Absorbance was measured at 565 nanometers (nm) using an Epoch Microplate Spectrophotometer (Agilent Technologies, Inc., Santa Clara, CA) with Gen5 Data Analysis software. The most consistent and accurate method for determining the protein concentrations over time is to prepare a large batch of diluted BSA standards, aliquot them into small portions, and store them frozen.

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