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Apolipoprotein AI

16-16-120101
Athens Research
Protein IDP02647
Product group Proteins / Signaling Molecules
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Overview

  • Supplier
    Athens Research
  • Product Name
    Apolipoprotein AI
  • Delivery Days Customer
    9
  • Applications Supplier
    In Vitro Diagnostic, Cardiovascular Research, ALS, Diabetes
  • Certification
    Research Use Only
  • Estimated Purity
    ≥95% by SDS-PAGE
  • Protein IDP02647
  • Protein Name
    Apolipoprotein A-I
  • Scientific Description
    Apolipoprotein AI (Apo AI), constituting 75% of HDL-associated apolipoproteins, is a critical for reverse cholesterol transport (RCT), mediating cholesterol efflux from peripheral tissues to the liver. As the primary structural component of HDL, Apo AI stabilizes discoidal HDL particles, activates lecithin-cholesterol acyltransferase (LCAT) to esterify cholesterol, and facilitates HDL maturatioN. Its anti-inflammatory properties include blocking T-cell–monocyte interactions, reducing TNF-alfa and IL-1bèta production, and neutralizing oxidized LDL. Normal plasma levels range from 90–130 mg/100 mL, with concentrations inversely correlating with coronary heart disease (CHD) risk. Deficiencies in Apo AI underlie Tangier disease, characterized by near-absent HDL, cholesterol-laden macrophages, and premature atherosclerosis. Mutations like APOA1 p.Leu202Arg cause systemic amyloidosis, leading to cardiac and renal dysfunction. Reduced Apo AI levels also associate with insulin resistance, impaired bèta-cell function, and diabetes progression. Conversely, Apo AI overexpression enhances macrophage-specific RCT, attenuating atherosclerosis.
  • Shelf life instruction
    more then 1 year
  • Source
    Source human plasma non-reactive for HBsAG, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.
  • Storage Instruction
    -80C
  • UNSPSC
    41116100

References

  • Prathipati, P., et al., (2016), 'Development of novel HDL-mimicking alfa-tocopherol-coated nanoparticles to encapsulate nerve growth factor and evaluation of biodistribution', Polym. Chem., 7: pp 3897.
    Read this paper
  • Tarlton, J. M. R., et al., (2021), 'Protection against Glucolipotoxicity by High Density Lipoprotein in Human PANC-1 Hybrid 1.1B4 Pancreatic Beta Cells: The Role of microRNA', Biology, 10: pp 218.
    Read this paper
  • Caridis, A. M., et al., (2019), 'Genetic obesity increases pancreatic expression of mitochondrial proteins which regulate cholesterol efflux in BRIN-BD11 insulinoma cells', Bioscience Reports (2019) 39(3): BSR20181155.
    Read this paper
  • Scharadin, T. M., et al., (2017), 'Synthesis and biochemical characterization of EGF receptor in a water-soluble membrane model system', PLoS ONE, 12(6): e0177761.
    Read this paper
  • Zheng, Y. Z., et al., (2017), 'Manipulating trypsin digestion conditions to accelerate proteolysis and simplify digestion workflows in development of protein mass spectrometric assays for the clinical laboratory', Clinical Mass Spectrometry, 6: pp 1–12.
    Read this paper