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Hexanoyl-Lysine Adduct (HEL) ELISA 试剂盒

人 Hexanoyl-Lysine Adduct (HEL) ELISA Kit, Colorimetric is an assay for quantification of 人 Hexanoyl-Lysine Adduct (HEL), that has been mentioned in 6+ publications.
产品编号 ABIN1020379
发货至: 中国
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Quick Overview for Hexanoyl-Lysine Adduct (HEL) ELISA 试剂盒 (ABIN1020379)

抗原

Hexanoyl-Lysine Adduct (HEL)

适用

检测方法

Colorimetric

实验类型

Competition ELISA

检测范围

2-700 nM/L

应用范围

ELISA

样品类型

Cell Culture Samples, Serum, Urine
  • 最低检测浓度

    2 nM/L

    原理

    ELISA kit has been developped, and HEL can be detected in oxidatively modified LDL, in human atherosclerotic lesions, human urine and serum.

    Analytical Method

    Quantitative

    特异性

    Specific to N-epsilon-Hexanoyl-Lysine adduct.

    产品特性

    Assay Time: Overnight and 2 hours

    组件

    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

    试剂未包括

    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)
  • 板类型

    Pre-coated

    限制

    仅限研究用
  • 储存条件

    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." in: 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." in: 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." in: 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." in: 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." in: 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." in: Bioscience, biotechnology, and biochemistry, Vol. 66, Issue 4, pp. 869-72, (2002) (PubMed).

  • 抗原

    Hexanoyl-Lysine Adduct (HEL)

    背景

    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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