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ALX-270-407 Revised 24-Jul-08
4-Oxo-2-nonenal
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SYNONYMS 4-ONE
PRODUCT LINE Oxidative Stress
PRODUCT CATEGORY Lipid Peroxidation
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-270-407-M001   1 mg 108.00 USD Add To Cart
ALX-270-407-M005   5 mg 483.00 USD Add To Cart
Product Specification
FORMULA: C9H14O2
MW: 154.2
CAS NUMBER: 103560-62-9
CONCENTRATION: 10mg/ml
PURITY: 98%
FORMULATION: Liquid. Solution in methyl acetate.
SOLUBILITY: 50mg/ml soluble in 100% ethanol, dimethyl formamide or DMSO; sparingly soluble in PBS, pH 7.2 (0.5mg/ml).
SHIPPING: SHIPPED ON DRY ICE
LONG TERM STORAGE: -80°C
USE/STABILITY: Stable for at least 6 months after receipt when stored at -80°C. Keep aqueous solutions on ice and use within 12 hours.

Product Description
Lipid peroxidation product. Modifies histidine and lysine residues in proteins and causes protein cross-linking, modifies 2'-deoxyguanosine, and implicates lipid peroxidation in mutagenesis and carcinogenesis.
Product Specific Literature References
Covalent modifications to 2'-deoxyguanosine by 4-oxo-2-nonenal, a novel product of lipid peroxidation: D. Rindgen, et al.; Chem. Res. Toxicol. 12, 1195 (1999) Abstract
Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation: S.H. Lee, et al.; Chem. Res. Toxicol. 13, 698 (2000) Abstract
Aldehydic lipid peroxidation products derived from linoleic acid: P. Spiteller, et al.; Biochem. Biophys. Acta 1531, 188 (2001) Abstract
Mass spectroscopic characterization of protein modification by 4-hydroxy-2-(E)-nonenal and 4-oxo-2-(E)-nonenal: Z. Liu, et al.; Chem. Res. Toxicol. 16, 901 (2003) Abstract
Model studies on protein side chain modification by 4-oxo-2-nonenal: W.H. Zhang, et al.; Chem. Res Toxicol. 16, 512 (2003) Abstract
Induction of apoptosis in colorectal carcinoma cells treated with 4-hydroxy-2-nonenal and structurally related aldehydic products of lipid peroxidation: J.D. West, et al.; Chem. Res. Toxicol. 17, 453 (2004) Abstract
General Information
BACKGROUND/TECHNICAL INFORMATION To change the solvent, evaporate the methyl acetate under a gentle stream of nitrogen and immediately add the solvent of choice. Further dilutions of the stock solution into aqueous buffers or isotonic saline should be made prior to performing biological experiments.
 
 

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