Mouse Monoclonal Superoxide Dismutase 1 antibody - conjugated to PE. Suitable for Flow Cyt (Intra) and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human SOD1 aa 1 to C-terminus.
Preservative: 0.09% Sodium azide
Constituents: 0.5% BSA
Flow Cyt (Intra) | |
---|---|
Human | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Use at 5 μl/Test |
Destroys radicals which are normally produced within the cells and which are toxic to biological systems.
Superoxide dismutase [Cu-Zn], Superoxide dismutase 1, hSod1, SOD1
Mouse Monoclonal Superoxide Dismutase 1 antibody - conjugated to PE. Suitable for Flow Cyt (Intra) and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human SOD1 aa 1 to C-terminus.
Preservative: 0.09% Sodium azide
Constituents: 0.5% BSA
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The oxidative stress defense proteins protect cells from damage induced by reactive oxygen species (ROS). These proteins including superoxide dismutase catalase and glutathione peroxidase counteract oxidative stress by neutralizing harmful ROS. Superoxide dismutase with a mass of approximately 32 kDa is expressed in the cytoplasm mitochondria and extracellular space across various tissues. Catalase and glutathione peroxidase play similar roles ensuring a balance is maintained in cellular environments prone to oxidative reactions.
These proteins engage with multiple cell processes to maintain cellular health by preventing oxidative damage to DNA proteins and lipids. These defense proteins often form part of larger complexes that work synergistically to reduce oxidative stress levels. By participating in antioxidant defense they limit cellular malfunction and support normal cellular signaling and function encompassing broad cellular protective mechanisms.
Proteins involved in oxidative stress defense play a role in the detoxification pathway reducing oxidative stress markers and maintaining cellular redox balance. The pathway involves interactions with key endogenous antioxidants like glutathione. They also intersect with inflammation-related pathways wherein oxidative stress-related damage often triggers inflammatory responses. Oxidative stress defense proteins may also interact with the nuclear factor erythroid 2-related factor 2 (Nrf2) a transcription factor important for inducing antioxidant response elements.
Oxidative stress defense proteins have connections to conditions such as neurodegenerative diseases like Alzheimer's and cardiovascular disorders. In Alzheimer's disease abnormal oxidation affects amyloid-beta proteins where oxidative stress exacerbates symptoms. Additionally oxidative stress influences pathways contributing to plaque formation in cardiovascular disease suggesting a role in disease progression. These proteins’ functions strongly tie to proteins like amyloid precursor protein in Alzheimer’s and low-density lipoprotein in cardiovascular disease emphasizing their critical role in disease pathophysiology.
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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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Intracellular flow cytometric analysis ofHeLa (human epithelial cell line from cervix adenocarcinoma) cells labeling Oxidative Stress Defense with ab275642 (Black) compared with isotype control (Grey).
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