Rabbit Polyclonal DMPO Nitrone Adduct antibody. Suitable for ELISA, WB and reacts with Chemical samples. Cited in 6 publications. Immunogen corresponding to Chemical / Small Molecule corresponding to DMPO Nitrone Adduct.
Constituents: Whole serum
ELISA | WB | |
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Chemical | Expected | Tested |
Species | Dilution info | Notes |
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Species Chemical | Dilution info 1/1000 - 1/5000 | Notes - |
Species | Dilution info | Notes |
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Species Chemical | Dilution info 1/1000 - 1/5000 | Notes - |
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55 dimethyl 1 pyrroline N oxide nitrone adduct
Rabbit Polyclonal DMPO Nitrone Adduct antibody. Suitable for ELISA, WB and reacts with Chemical samples. Cited in 6 publications. Immunogen corresponding to Chemical / Small Molecule corresponding to DMPO Nitrone Adduct.
Constituents: Whole serum
Measurement of protein radicals is now possible with the development of the "spin trap immunoassay" (please see refs 1,2). Compared to traditional techniques, immunodetection of spin trap products allows a higher level of sensitivity and throughput with greatly reduced sample consumption.
The DMPO nitrone adduct also known as 55-Dimethyl-1-Pyrroline N-Oxide adduct plays an important role in trapping free radicals during biological reactions. As a spin trap DMPO captures highly reactive radicals like hydroxyl and superoxide radicals converting them to more stable radical adducts that can be detected by Electron Spin Resonance (ESR) spectroscopy. The mass of the DMPO nitrone adduct varies depending on the specific radical bound but the core structure of DMPO nitrone has a molecular weight of 113.15 g/mol. DMPO adducts are expressed in conditioned systems and are especially useful in detecting radical species in cellular environments.
DMPO nitrone adduct formation is critical for investigating oxidative stress within cells. It does not form part of a complex but acts as an independent trap for free radicals. By stabilizing reactive radicals DMPO adducts help to provide a clearer picture of the radical landscape within biological systems. This insight is essential for understanding the balance between reactive oxygen species production and antioxidant defense mechanisms in various cell types and tissues.
DMPO nitrone adduct formation links closely to pathways involving oxidative stress and redox signaling. In these pathways DMPO assists in monitoring dynamic changes and interactions between radicals and antioxidant proteins like superoxide dismutase (SOD) and catalase. These pathways are important for maintaining cellular health and preventing oxidative damage.
The use of DMPO nitrone adduct is significant for research on oxidative stress-related conditions. It is connected to diseases like Alzheimer's and cardiovascular disorders where oxidative stress and free radical damage play a well-documented role. The formation of DMPO adducts provides a method for assessing the extent of radical involvement offering insights into disease mechanisms. The interaction between DMPO and proteins such as amyloid-beta in Alzheimer's highlights the importance of free radical monitoring in understanding disease progression.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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ab23702 was used at a concentration of 1/1000 or 1/5000, as noted at the top of the image.
All lanes: Western blot - Anti-DMPO Nitrone Adduct antibody (ab23702)
Lane 1: Metmyoglobin at 3 µL
Lane 2: Metmyoglobin-DMPO at 3 µL
Lane 3: Metmyoglobin-DMPO at 5 µL
Lane 4: Metmyoglobin-DMPO at 10 µL
Observed band size: 17 kDa
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