Oxidative Stress Defense (Catalase, SOD1, TRX, smooth muscle Actin) Western Blot Cocktail (ab179843) is part of the reagents, controls & accessories range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
WB
CAT
(See target data below)
Human
Liquid
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application WB | Reactivity Reacts | Dilution info - | Notes Antibody cocktail should be diluted to 1X in appropriate dilution buffer before use. WB samples should be heated to 95°C for 5 minutes in sample buffer before loading. Suggested dilution buffer is 5% milk/PBS+0.05%Tween 20. |
Catalyzes the degradation of hydrogen peroxide (H(2)O(2)) generated by peroxisomal oxidases to water and oxygen, thereby protecting cells from the toxic effects of hydrogen peroxide (PubMed:7882369). Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells (PubMed:7882369).
SOD1, TXN, ACTG2 acetyl E3
Catalase, CAT
Oxidative Stress Defense (Catalase, SOD1, TRX, smooth muscle Actin) Western Blot Cocktail (ab179843) is part of the reagents, controls & accessories range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
WB
CAT
Human
Liquid
Preservative: 0.01% Sodium azide
Constituents: Proprietary component, 50% Glycerol (glycerin, glycerine), 0.9% Sodium chloride, 0.6% Tris, 0.05% BSA
Blue Ice
+4°C
-20°C
This Oxidative Stress Defense Western Blot Cocktail is designed to determine the relative abundance of several important proteins involved in the protection of cells against oxidative stress and the regulation of reactive oxygen species (ROS). Reactive oxygen species' are produced naturally in cells as byproducts of the metabolism of oxygen as well as in response to various environmental stresses including UV radiation, pollutants, and heat exposure. Additionally, ROS levels can be altered by disease and injury, including cancer, neurodegenerative disease, cardiovascular disease, ischemia, stroke and aging. Reactive oxygen species also play an important role in cell signaling, a process called redox signaling. The regulation of ROS within cells is important for maintaining a proper homeostasis.
Superoxide dismutase 1 (SOD1) scavenges harmful superoxides (O2-) within cells protecting them from harmful oxidation of lipids, proteins and nucleic acids. Its altered expression levels have been linked to Down's syndrome, ALS and various cancers. Similarly, the hydrogen peroxide(H2O2) scavenging enzyme, catalase, also regulated ROS concentrations within cells by reducing H202 into less reactive O2 and water. Thioredoxin is a small enzyme (12kDa) that facilitates the reduction of other enzymes via cysteine thiol-disulfide exchange. Thioredoxin is used by cells to reduce ROS amounts and in redox signaling processes. Finally, alpha smooth muscle actin was included in the cocktail as a loading control. Widely expressed, smooth muscle actin is involved in cell structure and motility.
These four readouts are easily resolved by western blot given their different molecular weights. Because they are all rabbit monoclonal antibodies, an anti-rabbit secondary should be used for detection.
Expected and observed MWs:
WB Notes:
The cocktail contains 50% glycerol, can be stored at -20C. No aliquoting necessary.
Related products
Review the oxidative stress marker and assay guide to learn about more assays for oxidative stress.
This supplementary information is collated from multiple sources and compiled automatically.
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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Densiometric analysis of a western blot using ab179843 was used on various cell types to determine the relative amounts of catalase, superoxide dismutase 1 and thioredoxin.
25 ug of each cell lysate was loaded per lane after heating for 5 minutes at 95°C.
Lane 1: HepG2
Lane 2: HeLa
Lane 3: HDFn
Lane 4: HL60
Lane 5: Jurkat
Lane 6: MCF7
Lane 7: Hek293T
Secondary: HRP-conjugated Anti-Rabbit IgG
WB lysate sample was heated at 95°C for 5 minutes before loading. Performed under reducing conditions.
All blocking and antibody incubation steps were done in 5% milk in PBST.
Developed using the ECL technique.
Exposure time: 1 minute.
Sample: HepG2 Cell Lysate – 25 μg/lane
Lane 1: Anti-Catalase antibody
Lane 2: Anti-Smooth muscle actin antibody
Lane 3: Anti-Superoxide dismutase 1 antibody
Lane 4: Anti-Thioredoxin antibody
Lane 5: ab179843 Oxidative Stress Defense WB Cocktail
Secondary: HRP-conjugated Anti-Rabbit IgG
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