Protein Quantitation
Protein quantitation and protein assays are critical for accurately determining the protein concentration in a sample. There are a variety of protein quantitation methods including UV absorbance assays, reagent-based assays, and immunoassay technologies. Each of these protein quantitation technologies has unique benefits and the suitability of the assay depends on the sample type and/or volume that is available for analysis. For example, some of the dye-based assays may interfere with chemicals found in buffer preparations and an alternative assay may be more appropriate. Scientists need to consider the limitations of each assay to determine which is the best option for their sample.
UV Absorbance Assays
Using ultraviolet (UV) absorbance to measure protein concentration is a relatively simple protein quantitation assay. Amino acids with aromatic side chains (tryptophan, tyrosine, etc.) provide proteins with their distinctive UV absorbance at 280 nm. Because these amino acids absorb UV light at 280 nm, the absorbance at this particular wavelength can be obtained through a spectrophotometer and used to estimate protein concentrations in samples. This relatively quick assay is frequently used in laboratories and the Warburg-Christian method is typically performed for the protein concentration estimation. However, using UV absorbance for protein concentration may have high variability because non-protein components in a sample may interfere with absorbance measurements. Additionally, mixtures with different proteins in a sample could cause varying absorbance readings due to the difference in amino acid compositions.
Reagent-Based Assays
Reagent-based assays overcome the compatibility issues that are observed with UV absorbance methods. Examples of reagent-based assays for protein quantitation include those that utilize colorimetric methods, such as bicinchoninic acid (BCA), Lowry, and Bradford assays. The BCA method and the Lowry method both involve the formation of a copper-protein complex. These are sensitive assays and are less variable than the Bradford assay. However, the Bradford assay is rapid, easy to perform, and is compatible with certain reducing agents, unlike the BCA and Lowry assays.
Immunoassays
Some assays may not be able to support accurate protein quantitation if there are multiple proteins in a sample or quantities are below the detection threshold. Powerful immunoassay technologies, using various detection methods, provide an alternate method to precisely quantitate proteins from a variety of sample types. For example, multiplex assays allow researchers to quantitate multiple proteins in a sample simultaneously. In addition, single molecule counting technology can measure femtogram levels of proteins to help identify and quantify low-level proteins in small samples. Research applications using these technologies include measuring biomarkers in healthy tissues or those associated with disease progression to better understand certain disease states.
Visit our document search for data sheets, certificates and technical documentation.
Related Articles
- Learn more about Mass Spectrometry or MS including what it is, what it is used for and how it works.
- To standardize a procedure for the determination of protein by modified Lowry.
- A wide variety of products for traditional protein quantitation techniques such as BCA and Bradford. Also, products for alternative assays such as Lowry, Micro Pyrogallol and FluoroProfile are also available for total protein determination.
- Learn how total protein quantitation with an infrared spectrometer may be a more accurate and universal alternative to Bradford, BCA, or UV-based methods.
- This troubleshooting table lists problems that may be encountered in two-dimensional difference gel electrophoresis (2D DIGE) results, including possible causes and methods to prevent future problems.
- See All (21)
Related Protocols
- A standard procedure for the quantitative determination of total protein concentration of a solution by the BCA method.
- To determine protein content, the Warburg-Christian method refers to measuring protein samples at 280 nm using a spectrophotometer.
- 2-D Quant Kit from Cytiva is designed to accurately determine protein concentrations in samples for electrophoresis.
- See All (15)
Find More Articles and Protocols
How Can We Help
In case of any questions, please submit a customer support request
or talk to our customer service team:
Email custserv@sial.com
or call +1 (800) 244-1173
Additional Support
- Chromatogram Search
Use the Chromatogram Search to identify unknown compounds in your sample.
- Calculators & Apps
Web Toolbox - science research tools and resources for analytical chemistry, life science, chemical synthesis and materials science.
- Customer Support Request
Customer support including help with orders, products, accounts, and website technical issues.
- FAQ
Explore our Frequently Asked Questions for answers to commonly asked questions about our products and services.
To continue reading please sign in or create an account.
Don't Have An Account?