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Lipoprotein, Low Density, Oxidized

12-16-120412-OX
Athens Research
Product group Proteins / Signaling Molecules
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Overview

  • Supplier
    Athens Research
  • Product Name
    Lipoprotein, Low Density, Oxidized
  • Delivery Days Customer
    9
  • Applications Supplier
    Cell Culture Media, In Vitro Diagnostics, Assay Development, Cardiovascular Disease, Diabetes, Inflammation, Oxidative Stress
  • Certification
    Research Use Only
  • Estimated Purity
    ≥ 95% by electrophoresis
  • Scientific Description
    Oxidized low-density lipoprotein (Ox-LDL) is a modified form of LDL in which both the lipid and protein components, particularly apolipoprotein B-100, undergo oxidative changes. These modifications include the formation of aldehydes, cross-linking of amino acids, and the generation of new antigenic epitopes, making Ox-LDL structurally and functionally distinct from native LDL. Functionally, Ox-LDL is recognized and taken up by macrophage scavenger receptors, leading to foam cell formation-a key step in atherogenesis. Ox-LDL also acts as a cytotoxin, injuring endothelial cells, increasing endothelial permeability, and promoting inflammatory responses, which further contribute to vascular dysfunction and lesion development. Clinically, elevated levels of Ox-LDL are strongly associated with atherosclerosis, metabolic syndrome, type 2 diabetes, and coronary heart disease. Ox-LDL is implicated in the progression of these diseases due to its pro-inflammatory and cytotoxic effects on vascular cells. In research and diagnostics, Ox-LDL is used to study cellular responses to oxidative stress, to assess cardiovascular risk, and as a probe in assays such as ELISA, Western blot, and fluorescence microscopy to track its uptake and effects in biological systems.
  • Shelf life instruction
    more then 6 months from the production date
  • Source
    Prepared from fresh, non-frozen plasma shown to be non reactive for HBsAg, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA-required tests.
  • Storage Instruction
    +2 - 8° C
  • UNSPSC
    12352202

References

  • Dai, X., et al., (2017), 'Elevating CXCR7 Improves Angiogenic Function of EPCs via Akt/GSK-3bèta/Fyn-Mediated Nrf2 Activation in Diabetic Limb Ischemia', Circ Res. 120: pp e7-e23.
    Read this paper
  • Pham, L. M., et al., (2021), 'Targeting and clearance of senescent foamy macrophages and senescent endothelial cells by antibody-functionalized mesoporous silica nanoparticles for alleviating aorta atherosclerosis', Biomaterials 269: pp 120677
    Read this paper
  • Chen, J., et al., (2024), ' Atherosclerotic three-layer nanomatrix vascular sheets for high-throughputtherapeutic evaluation', Biomaterials 305: pp 122450
    Read this paper
  • Zhu, Y., et al., ( 2025), 'Oxidative stress promotes lipid-laden macrophage formation via CYP1B1', Redox Biology 79: pp 103481
    Read this paper
  • Tan, L. X., et al., (2016), 'Protective responses to sublytic complement in the retinal pigment epithelium', PNAS August 2, 113(31): pp 8789-8794.
    Read this paper