A7785
Apolipoprotein C-I from human plasma
≥95% (SDS-PAGE), lyophilized powder
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About This Item
Produits recommandés
Source biologique
human
Niveau de qualité
Pureté
≥95% (SDS-PAGE)
Forme
lyophilized powder
Poids mol.
average mol wt 6.6 kDa
Technique(s)
inhibition assay: suitable
Numéro d'accès UniProt
Température de stockage
−20°C
Informations sur le gène
human ... APOC1(341)
Description générale
Very low density lipoprotein.
Application
Apolipoprotein C-1 directly interferes with fatty acid uptake and is a major plasma inhibitor of cholesterol ester transfer protein. Apolipoprotein C-I has been used to develop a quantitative strategy, named secretome-derived isotopic tag (SDIT), to concurrently identify and quantify the adipocyte-secreted plasma proteins from normal and high-fat-diet (HFD) induced obese mice.
Actions biochimiques/physiologiques
Interferes directly with fatty acid uptake and is the major plasma inhibitor of cholesterol ester transfer protein.
Forme physique
Lyophilized from 10 mM NH4HCO3, pH 7.5
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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The Biochemical journal, 178(2), 455-466 (1979-02-15)
1. The work reported was designed to provide quantitative information about the capacity of the extrahepatic tissues of the rat to degrade injected VLD lipoproteins (very-low-density lipoproteins, d less than 1.006) to LD lipoproteins (low-density lipoproteins, d 1.006--1.063) and to
Journal of proteome research, 11(5), 2851-2862 (2012-03-13)
We developed a quantitative strategy, named secretome-derived isotopic tag (SDIT), to concurrently identify and quantify the adipocyte-secreted plasma proteins from normal and high-fat-diet (HFD) induced obese mice, based on the application of isotope-labeled secreted proteins from cultured mouse adipocytes as
Biochemistry, 51(6), 1238-1248 (2012-01-24)
Apolipoprotein C-I (apoC-I) is an important constituent of high-density lipoprotein (HDL) and is involved in the accumulation of cholesterol ester in nascent HDL via inhibition of cholesterol ester transfer protein and potential activation of lecithin:cholesterol acyltransferase (LCAT). As the smallest
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