Apolipoprotein AI
16-16-120101-LEL
Protein IDP02647
Product group Proteins / Signaling Molecules
Overview
- SupplierAthens Research
- Product NameApolipoprotein AI
- Delivery Days Customer9
- Applications SupplierIn Vitro Diagnostic, Cardiovascular Research, ALS, Diabetes, Cell Based Assays, Animal Studies
- CertificationResearch Use Only
- Estimated Purity≥95% by SDS-PAGE
- Protein IDP02647
- Protein NameApolipoprotein A-I
- Scientific DescriptionApolipoprotein 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 instructionmore then 1 year
- SourceSource human plasma non-reactive for HBsAG, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.
- Storage Instruction-80C
- UNSPSC41116100
References
- Deng, M. et al., (2018), 'LILRB4 signalling in leukaemia cells mediates T cell suppression and tumour infiltration', Nature, 562: pp 605–609.Read this paper
- Garbuzova-Davis, et al., (2022), 'Apolipoprotein A1 Enhances Endothelial Cell Survival in an In Vitro Model of ALS', eNeuro, 9(4): ENEURO.0140-22.2022.Read this paper