NOTICE: Due to a lapse in annual appropriations, most of this website is not being updated. Learn more.
Form submissions will still be accepted but will not receive responses at this time. Sections of this site for programs using non-appropriated funds (such as NVLAP) or those that are excepted from the shutdown (such as CHIPS and NVD) will continue to be updated.
An official website of the United States government
Here’s how you know
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
Secure .gov websites use HTTPS
A lock (
) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.
QconCAT: Internal Standard for Protein Quantification
Published
Author(s)
Kerry M. Bauer, Karen W. Phinney, Illarion V. Turko
Abstract
Protein quantification based on stable-isotope labeling mass spectrometry (SIL-MS) involves adding known quantities of stable-isotope labeled internal standards into biological samples. The internal standards are analogous to analyte molecules and quantification is achieved by comparing signals from isotope-labeled and analyte molecules. This methodology is broadly applicable to proteomics research, biomarker discovery and validation, and clinical studies; which require accurate and precise protein abundance measurements. One such internal standard platform for protein quantification are concatenated peptides (QconCAT). This paper describes a protocol for the design, expression, characterization, and application of the QconCAT strategy for protein quantification.
QconCAT, stable isotope labeling, mass spectrometry, proteomics, protein quantification, protocol
Citation
Bauer, K.
, Phinney, K.
and Turko, I.
(2015),
QconCAT: Internal Standard for Protein Quantification, Isotope labeling of biomolecules Part A & B, Methods in Enzymology (Elsevier), Oxford, -1, [online], https://doi.org/10.1016/bs.mie.2015.09.022
(Accessed October 9, 2025)