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.
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Catalog Number
Description
23275
Quantitative Colorimetric Peptide Assay
23290
Quantitative Fluorometric Peptide Assay
23295
Peptide Digest Assay Standard (1 mg/mL)
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Catalog number 23275
Price (USD)
478.00
Each
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Description:
Quantitative Colorimetric Peptide Assay
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Price (USD)
478.00
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 MethodColorimetric
FormatKit
Workflow StepIn-Process Testing
Quantity500 Assays
Unit SizeEach
Contents & Storage
Colorimettric Assay Reagent A, 50 mL Colorimetric Assay Reagent B, 2 x 25 mL Colorimetric Assay Reagent C, 2 mL Peptide Digest Assay Standard, 1.5 mL
Store in refrigerator (2–8°C).
Frequently asked questions (FAQs)
In the SMOAC protocol (https://www.thermofisher.com/blog/learning-at-the-bench/wp-content/uploads/sites/13/2024/10/High-SelectTM-SMOAC-Protocol.pdf), can I enrich with High-Select Fe-NTA kit first?
No. It is important to enrich with the TiO2 kit (Cat. No. A32993) first. Afterwards, the flow-through and wash fractions from this enrichment can be processed with the Fe-NTA kit (Cat. No. A32992). If this order is reversed (that is, Fe-NTA before TiO2), there will be 2 consequences as follows:
1. There will not be any significant additional recovery of peptides (maybe just a few more peptides).
2. There will be no enrichment for the multiple phosphorylated peptides, so those would be lost.
Why do you offer two phosphopeptide enrichment kits: the High-Select TiO2 kit (Cat. No. A32993) and the High-Select Fe-NTA kit (Cat. No. A32993)?
The two phosphopeptides enrichment kits, Fe-NTA and TiO2, enrich a complementary set of phosphopeptides.
Our R&D has developed a Sequential enrichment of Metal Oxide Affinity Chromatography (see https://assets.thermofisher.com/TFS-Assets/CMD/posters/PO-65032-SMOAC-Phosphoproteomics-Peptides-ASMS2017-PO65032-EN.pdf and https://www.thermofisher.com/blog/learning-at-the-bench/wp-content/uploads/sites/13/2024/10/High-SelectTM-SMOAC-Protocol.pdf?CID=bid_mic_r04_jp_cp0000_pjt0000_bid00000_0so_blg_protein_analysis_mass_spectrometry_bid_ts_mbr_24065_Social_LAB) where flow-through and wash fractions from TiO2 enrichment were combined and subjected to Fe-NTA enrichment. This sequential enrichment provides impressive coverage of phosphoproteomes.
What are the differences between the old Fe-NTA kit (Cat. No. 88300) and the new High-Select Fe-NTA kit (Cat. No. A32992)?
There are four differences between the Fe-NTA kit (Cat. No. 88300) and the new High-Select Fe-NTA kit (Cat. No. A32992) kit as follows:
1. The selectivity - the ratio of number of phosphopeptides over total peptides - was significantly improved to 99% with Cat. No. A32992, because the reagents were extensively optimized for the phosphopeptide selection.
2. The phosphopeptide yield was also increased to 33 µg based on quantitative colorimetric peptide assay (Cat. No. 23275).
3. The reagent is a pre-formulated format, so mixing reagent to prepare the working solution from stock solutions provided in the old kit (Cat. No. 88300) is not necessary, so it is easier to handle.
4. The enrichment protocol is optimized and streamlined, which means there are many fewer steps than with Cat. No. 88300. Thus, it takes <45 min to finish the entire protocol compared to 2 hours with the old kit (Cat. No. 88300).
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.