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Hexanoyl-Lysine Adduct (HEL) Kit ELISA

Reactivité: Humain Colorimetric Competition ELISA 2-700 nM/L Cell Culture Samples, Serum, Urine
N° du produit ABIN1020379
  • Antigène
    Hexanoyl-Lysine Adduct (HEL)
    Reactivité
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Gamme de detection
    2-700 nM/L
    Seuil minimal de détection
    2 nM/L
    Application
    ELISA
    Fonction
    ELISA kit has been developped, and HEL can be detected in oxidatively modified LDL, in human atherosclerotic lesions, human urine and serum.
    Type d'échantillon
    Cell Culture Samples, Serum, Urine
    Analytical Method
    Quantitative
    Specificité
    Specific to N-epsilon-Hexanoyl-Lysine adduct.
    Attributs du produit
    Assay Time: Overnight and 2 hours
    Ingrédients
    HEL-coated Microtiter Plate: 1 plate (96 wells)
    Primary Antibody (ready to use): 1 vial
    Secondary Antibody: 1 vial
    Secondary Antibody Buffer: 1 vial
    Chromogen (TMBZ solution): 1 vial
    Chromogen Buffer: 1 vial
    Washing Buffer (5X): 1 vial
    Stop Solution: 1 vial
    Standard solution (6 levels): 1 vial each
    Plate seal: 2 sheets
    Matériel non inclus
    50 µL micropipettor and pipette tips 8-channel (50-200 µL) micropipettor and tips 8 or 12-syncronous multichannel pipet and reagent tray for multichannel pipet. 4-7°C incubator Microtiter plate reader (measuring wavelength 450 nm)
  • Plaque
    Pre-coated
    Restrictions
    For Research Use only
  • Stock
    4 °C
  • Sugiyama, Sun, Nishinohara, Fujita, Masuda, Ochi, Takeuchi: "Expressions of lipid oxidation markers, N(ε)-hexanoyl lysine and acrolein in cisplatin-induced nephrotoxicity in rats." dans: The Journal of veterinary medical science / the Japanese Society of Veterinary Science, Vol. 73, Issue 6, pp. 821-6, (2011) (PubMed).

    Wakamatsu, Dogru, Ayako, Takano, Matsumoto, Ibrahim, Okada, Satake, Fukagawa, Shimazaki, Tsubota, Fujishima: "Evaluation of lipid oxidative stress status and inflammation in atopic ocular surface disease." dans: Molecular vision, Vol. 16, pp. 2465-75, (2010) (PubMed).

    Shimizu, Ogawa, Akiyama, Muroi, Yoshizaki, Iwata, Komura, Bae, Sato: "Increased serum levels of N(epsilon)-(hexanoyl)lysine, a new marker of oxidative stress, in systemic sclerosis." dans: The Journal of rheumatology, Vol. 35, Issue 11, pp. 2214-9, (2008) (PubMed).

    Suzuki, Kazui, Yamamoto, Washiyama, Ohkura, Ohishi, Bashar, Yamashita, Terada, Suzuki, Akuzawa, Fujie: "Effect of prophylactically administered edaravone during antegrade cerebral perfusion in a canine model of old cerebral infarction." dans: The Journal of thoracic and cardiovascular surgery, Vol. 133, Issue 3, pp. 710-6, (2007) (PubMed).

    Naito, Wu, Nomura, Kodama, Kato, Kato, Osawa: "The protective effects of tetrahydrocurcumin on oxidative stress in cholesterol-fed rabbits." dans: Journal of atherosclerosis and thrombosis, Vol. 9, Issue 5, pp. 243-50, (2002) (PubMed).

    Ueno, Horio, Uchida, Naito, Nomura, Kato, Tsuda, Toyokuni, Osawa: "Increase in oxidative stress in kidneys of diabetic Akita mice." dans: Bioscience, biotechnology, and biochemistry, Vol. 66, Issue 4, pp. 869-72, (2002) (PubMed).

  • Antigène
    Hexanoyl-Lysine Adduct (HEL)
    Sujet
    Oxidative damage of lipids caused by reactive oxygen species (ROS) play an important role in some diseases, lesion of cell functions and aging. Aldehydes such as malondi-aldehyde (MDA) and 4-hydroxy-2-nonenal (4-HNE) have been reported as one of the advanced lipid peroxidation products. But recently in the earlier stage of lipid peroxidation, 13-hydroperoxyoctadecanoic acid (13-HPODE) is found to be covalently bound to proteins1). Hexanoyl-Lysine adduct (HEL) is a novel lipid hydroperoxide-modified lysine residues. HEL is formed by oxidative modification by oxidized omega-6 fatty acids such as linoleic acid or arachidonic acid. HEL may be a useful biomarker for initial stage of lipid peroxidation.Monoclonal antibodies and ELISA kit have been developped, and HEL can be detected in oxidatively modified LDL, in human atherosclerotic lesions, human urine and serum. It is also reported that HEL is formed in rat muscle during exercise, and the formation is prohibited by antioxidants such as flavonoids.
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