Mouse Monoclonal Acrolein antibody. Suitable for WB, Flow Cyt and reacts with Chemical samples. Cited in 1 publication. Immunogen corresponding to Chemical / Small Molecule corresponding to Acrolein.
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
WB | Flow Cyt | |
---|---|---|
Chemical | Tested | Tested |
Species | Dilution info | Notes |
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Species Chemical | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
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Species Chemical | Dilution info 1/50 | Notes - |
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2-Propen-1-one, 2-propenal, Acraldehyde, Acrylic aldehyde
Mouse Monoclonal Acrolein antibody. Suitable for WB, Flow Cyt and reacts with Chemical samples. Cited in 1 publication. Immunogen corresponding to Chemical / Small Molecule corresponding to Acrolein.
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
Specific for Acrolein modified proteins. Does not detect free acrolein. Does not X-react with Crotonaldehyde, Hexanoyl Lysine, 4-HHE, 4-HNE, MDA, or Methylglyoxal modified proteins.
Acrolein also known as acraldehyde is a highly reactive aldehyde with a molecular weight of 56.06 g/mol. It is a volatile compound commonly found in the environment resulting from combustion processes and as a metabolite of certain drugs and chemicals. At physiological levels acrolein is present in various tissues and cells primarily within the liver where it is generated through lipid peroxidation. It is noteworthy that acrolein does not typically function as a singular enzyme or protein but regulates through its interaction with cellular components.
Interactions of acrolein with cellular macromolecules such as proteins and DNA occur due to its electrophilic nature. It readily forms adducts leading to structural changes and potentially harmful effects on cellular mechanisms. While it is not part of a larger complex acrolein's formation of adducts significantly alters protein function and gene expression. This reactivity with biological molecules plays an important role in modulating signaling pathways and cellular responses.
Interactions involving acrolein affect oxidative stress and inflammation pathways. The compound modifies important proteins like NF-kappaB a transcription factor involved in the immune and inflammation responses. Acrolein's influence on lipid peroxidation links it to the arachidonic acid pathway where it affects processes like prostaglandin synthesis. Associated proteins in these pathways include COX-2 and LOX which play roles in modulating inflammation.
Acrolein's biological interactions have implications in conditions such as cardiovascular disease and cancer. The aldehyde contributes to cardiovascular pathology by damaging endothelial cells and promoting atherosclerosis. Similarly acrolein exposure and its role in DNA damage can facilitate oncogenic processes making it a relevant factor in cancer development. Its connection with proteins like p53 in cancer pathways underlines acrolein's contribution to disease progression and its potential as a target for therapeutic intervention.
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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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Block: 5% Skim Milk in 1X TBST.
Primary incubation for 2 hours at room temperature.
Secondary incubation for 1 hour at room temperature.
All lanes: Western blot - Anti-Acrolein antibody [2H2] (ab240906) at 1/1000 dilution
Lane 1: ab245924 at 1 µg
Lane 2: ab245924 at 0.5 µg
Lane 3: ab245924 at 0.1 µg
All lanes: Goat Anti-Mouse IgG: HRP at 1/2000 dilution
Developed using the ECL technique.
Predicted band size: 69 kDa
Exposure time: 5min
Flow cytometric analysis of 90% Methanol-fixed SH-SY5Y (human neuroblastoma cell line from bone marrow) cells using ab240906 at 1/50 dilution for 30 minutes on ice (solid line) compared to a control IgG (dotted line). Goat Anti-Mouse PE at 1/100 dilution for 20 min at RT was used as the secondary antibody.
Cells were subject to oxidative stress by treating with 250 μM H2O2 for 24 hours.
All lanes: Western blot - Anti-Acrolein antibody [2H2] (ab240906) at 1/1000 dilution
Lane 1: Acrolein-BSA at 0.5 µg
Lane 2: Acrolein-BSA at 2 µg
Lane 3: BSA at 0.5 µg
Lane 4: BSA at 2 µg
All lanes: Goat Anti-Mouse IgG: HRP at 1:2000 for 60 min at RT
Developed using the ECL technique.
Exposure time: 5min
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