Protein Carbonyl ELISA Kit
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(12 Publications)
- I-ELISA
Supplier Data
Indirect ELISA - Protein Carbonyl ELISA Kit (AB238536)
Amount of Protein Carbonyl Content for Cell Lysate and BSA Standard.
STO (MEF), HeLa and MDA-231 cells were sonicated in 25mM HEPES, pH 7.5, 150 mM NaCl, 10 mM MgCl2, 1 mM EDTA, 2% Glycerol. Cell Lysates and BSA Standard from Pierce BCA Protein Assay were diluted to 10 μg/mL with 1X PBS and coated onto a 96-well Protein Binding Plate. The protein carbonyl levels were determined as described in the Protein Carbonyl ELISA Protocol.
- I-ELISA
Supplier Data
Indirect ELISA - Protein Carbonyl ELISA Kit (AB238536)
Typical Protein Carbonyl ELISA Standard Curve.
This standard curve is for demonstration only. A standard curve must be run with each protein carbonyl elisa experiment.
Product details
Protein Carbonyl ELISA Kit (ab238536) is designed for the quantitative measurement of protein carbonyls in plasma, serum, cell lysates or purified proteins.
With this kit protein samples are first allowed to adsorb to wells of a 96-well plate and then react with dinitrophenylhydrazine (DNPH), which allows for derivatization of the carbonyl group. There are no concentration or precipitation steps, that contribute to sample loss. The kit allows detection of as little as 10 ug/mL using a standard microplate reader. The quantity of protein carbonyls in protein sample is determined by comparing its absorbance with that of a known reduced/oxidized BSA standard curve.
What's included?
Properties and storage information
Shipped at conditions
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Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Protein carbonylation alters protein function and structure. This process disrupts protein-protein interactions and impairs enzyme activity leading to protein dysfunction. Carbonylated proteins fail to perform effectively within cellular systems and accumulate in cells. These accumulations can form large aggregates which cells often recognize as damaged. Protein degradation systems struggle to efficiently degrade these aggregates which can lead to further cellular dysfunction.
Pathways
Protein carbonylation integrates into the oxidative stress response pathways. In particular it affects the proteostasis network by challenging the protein quality control systems which include chaperones and proteasomes. This can influence pathways like the ubiquitin-proteasome pathway as proteins like ubiquitin tag damaged proteins for degradation. Additionally carbonylated proteins intertwined with inflammatory pathways interact with proteins such as nuclear factor kappa B (NF-kB) contributing to pro-inflammatory signaling.
Product protocols
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Publications (12)
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Biology of sport 42:137-144 PubMed39758177
2025
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Antioxidants (Basel, Switzerland) 13: PubMed39456511
2024
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International journal of molecular sciences 25: PubMed38338809
2024
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GeroScience 45:3549-3560 PubMed37498479
2023
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International journal of molecular sciences 24: PubMed37446125
2023
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Scientific reports 13:8304 PubMed37221295
2023
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Toxics 11: PubMed36668787
2023
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 9:e2203242 PubMed36002317
2022
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Antioxidants (Basel, Switzerland) 11: PubMed35326118
2022
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Biology 11: PubMed35205143
2022
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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