Pierce colorimetric or fluorescent quantitative peptide assays and standards are easy-to-use microplate assays designed specifically to improve the sensitivity and reproducibility of peptide quantitation for use with mass spectrometry analysis.
Have Questions?
Change view
Catalog Number
Description
23290
Quantitative Fluorometric Peptide Assay
23275
Quantitative Colorimetric Peptide Assay
23295
Peptide Digest Assay Standard (1 mg/mL)
3 Options
Catalog number 23290
Price (USD)
520.00
Each
Add to cart
Description:
Quantitative Fluorometric Peptide Assay
Request bulk or custom format
Price (USD)
520.00
Each
Add to cart
Pierce colorimetric or fluorescent quantitative peptide assays are easy mix-and-read microplate assays with stable signals for accurate and robust measurement of peptide digest samples. A high-quality peptide digest reference standard is provided as a stand-alone, or in the kits for use in the generation of linear standard curves for improved accuracy and reproducibility. The increased sensitivity, low sample assay volume, and included reference standard are essential for accurate and robust measurement of peptide digest samples for normalization of sample injection amount for MS analysis.
• Sensitive—accurately detect as little as 5 μg/mL (fluorometric) or 25 μg/mL (colorimetric) of peptide mixture • Reproducible—assay performance rigorously tested using peptide digest mixtures • Robust peptide digest standard—kit includes a validated peptide digest standard for improved reproducibility of quantitation • Compatible—works with many reagents, including MS sample preparation reagents and TMT-labeled peptides (fluorometric assay) • Convenient—easy, mix-and-read format with stable signal that may be read in as little as 5 minutes (fluorometric) or 15 minutes (colorimetric)
Pierce Quantitative Colorimetric Peptide Assay provides modified BCA reagents for the reduction of Cu+2 to Cu+1, a proprietary chelator optimized for the quantitation of peptide mixtures, and peptide digest reference standard for use in the generation of control linear standard curves. This colorimetric peptide assay requires a small amount of sample (20 μL) and has a working peptide concentration range of 25–1000 μg/mL. In the reaction, the copper is first reduced by the amide backbone of peptides under alkaline conditions (Biuret reaction), followed by the chelator coupling with the reduced copper to form a bright red complex (absorbs at 480 nm) that can be read in as little as 15 minutes. The signal produced from this reaction is 3–4 fold more sensitive than the Micro-BCA Protein Assay for peptide analysis. Colorimetric peptide assay is compatible with TMT-labeled peptides but is not recommended for synthetic peptides because the assay is affected by peptide amino acid content.
Pierce Quantitative Fluorescent Peptide Assay reagents include peptide assay buffer, fluorescent peptide labeling reagent, and a peptide digest assay standard for the quantitative measurement of peptide concentrations. This sensitive assay requires only 10 μL of sample, produces a linear response with increasing peptide concentrations (5–1000 μg/mL), and results in a stable final fluorescence that can be detected in as little as 5 minutes. In this assay, peptides are specifically labeled at the amino-terminus using an amine-reactive fluorescent reagent that is non-fluorescent until reacted with tryptic peptides. The fluorescently labeled peptides are detected on a microplate reader (ex390/em475). This assay is suitable for the quantitative measurement of peptide digest mixtures and synthetic peptides with an unblocked amino terminus. Fluorescent assays are not compatible with TMT-labeled peptides.
Thermo Scientific Peptide Digest Assay Standard was designed as a reference standard for use with the Pierce quantitative fluorometric and colorimetric peptide assays to improve reproducibility and accuracy of peptide quantitation. The Peptide Digest Assay Standard is provided in ready-to-use liquid format at 1 mg/mL. The reference protein has been digested with MS-grade trypsin to minimize missed cleavages. To help ensure consistent performance, digestion efficiency of the protein is monitored to help ensure lot-to-lot consistency, and quality is assessed by comparison to a reference standard.
Applications • Normalizing sample concentrations for quantitative downstream applications • Normalizing sample loading volumes for LC, MS, and LC/MS applications • Measuring recovery after peptide clean-up procedures
For Research Use Only. Not for use in diagnostic procedures.
Starting MaterialPeptides, Protease-digested Protein
Final Product TypePeptides
Detection MethodFluorescence
FormatKit
Workflow StepIn-Process Testing
Quantity500 Assays
Unit SizeEach
Contents & Storage
Fluorometric Peptide Assay Reagent, 4 x 2.5 mL Fluorometric Peptide Assay Buffer, 50 mL Peptide Digest Assay Standard, 1.5 mL
Store in refrigerator (2–8°C).
Frequently asked questions (FAQs)
When I quantitate my mass spec peptide sample with the Pierce Quantitative Colorimetric Peptide Assay, I get different results than when I use the Pierce Quantitative Fluorometric Peptide Assay. Which is best to use for the most accurate quantitation?
Since the different peptide assays use different chemistries to measure peptides, they may result in different results. Interfering compounds are the most common source of background and inaccurate measurements. Please note that the fluorometric peptide assay is not recommended for peptides which have been modified using TMT reagents.
How can I determine peptide yield in my mass spectrometry samples after sample clean-up?
Peptide yield can be measured using the Pierce Quantitative Colorimetric Peptide Assay (Cat. No. 23275) or the Pierce Quantitative Fluorometric Peptide Assay (Cat. No. 23290). The choice of peptide assay depends on the sample type and composition of the sample buffer. The fluorometric peptide assay cannot be used to measure peptides with chemically modified amines such as acetylated peptides or TMT-labeled protein digests. The colorimetric assay can measure a wider range of samples but is not as sensitive as the fluorometric assay, requiring more sample for accurate detection. Finally, both assays are susceptible to interfering compounds in the sample or buffer which should be avoided or removed for best results.
I have good peptide identification numbers but the variation between sample replicates is high. What do you recommend to improve sample reproducibility?
We recommend reviewing your sample-prep workflow to ensure consistent protein extraction, reduction/alkylation, digestion, and clean-up. We recommend using EasyPep products for high quality, reproducible sample preparation (EasyPep Maxi Sample Prep Kit, EasyPep Mini MS Sample Prep Kit, EasyPep 96 MS Sample Prep Kit). We also recommend quantifying peptides using the Pierce Quantitative Fluorometric Peptide Assay (Cat. No. 23290) or Pierce Quantitative Coloimetric Peptide Assay (Cat. No. 23275) to ensure that the same amount of peptides are being used for each LC-MS analysis. Poor reproducibility could also be related to the LC-MS system performance which may require recalibration using Pierce Calibration Solutions. System performance can be assessed using protein digest standards such as Pierce HeLa Protein Digest Standard or Pierce TMT11plex Yeast Digest Standard and peptide standards such as Pierce Peptide Retention Time Calibration Mixture or Pierce LC-MS/MS System Suitability Standard (7 x 5 Mix).