Pierce™ Quantitative Peptide Assays & Standards
Pierce™ Quantitative Peptide Assays & Standards
Thermo Scientific™

Pierce™ Quantitative Peptide Assays & Standards

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 NumberProduct TypeDetection Method
23275Peptide AssayColorimetric
23290Peptide AssayFluorescence
23295Peptide Digest Assay StandardColorimetric, Fluorescence
Catalog number 23275
Price (EUR)
465,65
Online Exclusive
522,00
Save 56,35 (11%)
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Product Type:
Peptide Assay
Detection Method:
Colorimetric
Request bulk or custom format
Price (EUR)
465,65
Online Exclusive
522,00
Save 56,35 (11%)
Each
Add to cart
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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.
Specifications
Final Product TypePeptides
For Use With (Equipment)Microplate Reader
Quantity500 Assays
Workflow StepIn-Process Testing
Detection MethodColorimetric
FormatKit
Product LinePierce™
Product TypePeptide Assay
Starting MaterialPeptides, Protease-digested Protein
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).
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3230613ACertificate of AnalysisJun 27, 202523290
3230613Certificate of AnalysisJun 27, 202523290
3216866ACertificate of AnalysisJun 25, 202523290
3216866Certificate of AnalysisJun 25, 202523290
3216049Certificate of AnalysisJun 14, 202523295
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Safety Data Sheets

Frequently asked questions (FAQs)

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.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

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.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

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).

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

The solvent for the Pierce Quantitative Peptide Assays & Standards (Cat. No. 23275) is 50mM ammonium bicarbonate.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Quantitation Support Center.

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.

Find additional tips, troubleshooting help, and resources within our Mass Spectrometry Support Center.

Citations & References (9)

Citations & References
Abstract
The effect of altered pH growth conditions on the production, composition, and proteomes of Helicobacter pylori outer membrane vesicles.
Authors:Johnston EL,Guy-Von Stieglitz S,Zavan L,Cross J,Greening DW,Hill AF,Kaparakis-Liaskos M
Journal:Proteomics
PubMed ID:37991474
Gram-negative bacteria release outer membrane vesicles (OMVs) that contain cargo derived from their parent bacteria. Helicobacter pylori is a Gram-negative human pathogen that produces urease to increase the pH of the surrounding environment to facilitate colonization of the gastric mucosa. However, the effect of acidic growth conditions on the production ... More
Detectability of Biotin Tags by LC-MS/MS.
Authors:Nierves L,Lange PF
Journal:Journal of proteome research
PubMed ID:33780260
The high affinity of biotin to streptavidin has made it one of the most widely used affinity tags in proteomics. Early methods used biotin for enrichment alone and mostly ignored the biotin-labeled peptide. Recent advances in labeling have led to an increase in biotinylation efficiency and shifted the interest to ... More
Quantitative proteomic analysis of human peripheral nerves from subjects with type 2 diabetes.
Authors:Ising E,Åhrman E,Thomsen NOB,Eriksson KF,Malmström J,Dahlin LB
Journal:Diabetic medicine : a journal of the British Diabetic Association
PubMed ID:34309080
AIMS: Diabetic peripheral neuropathy (DPN) is a common and severe complication to type 2 diabetes. The pathogenesis of DPN is not fully known, but several pathways and gene polymorphisms contributing to DPN are described. DPN can be studied using nerve biopsies, but studies on the proteome of the nerve itself, ... More
Proteomics analysis reveals the differential impact of the p97 inhibitor CB-5083 on protein levels in various cellular compartments of the HL-60 cell line.
Authors:Huang W,Qiu Y,Huynh D,Wang TY,Chou TF
Journal:microPublication biology
PubMed ID:39677520
Human p97/VCP is a vital AAA ATPase (ATPase associated with diverse cellular activity) that plays critical roles in protein homeostasis by regulating autophagy, endosomal trafficking, and the ubiquitin-proteasome system. Global proteomics analysis of p97/VCP inhibition with CB-5083 has been performed in HCT116 colon cells. Here, we examined the impact of ... More
Response of Lactiplantibacillus plantarum NMGL2 to Combinational Cold and Acid Stresses during Storage of Fermented Milk as Analyzed by Data-Independent Acquisition Proteomics.
Authors:Zhang M,Yao M,Lai T,Zhao H,Wang Y,Yang Z
Journal:Foods (Basel, Switzerland)
PubMed ID:34209263
To understand the mechanism of tolerance of lactic acid bacteria (LAB) during cold storage of fermented milk, 31 LAB strains were isolated from traditional fermented products, and Lactiplantibacillus plantarum NMGL2 was identified with good tolerance to both cold and acid stresses. Data-independent acquisition proteomics method was employed to analyze the ... More
9 total citations

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