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Cholesteryl oleate-13C18

Original price was: $2,995.00.Current price is: $1,495.00.

Catalog Number: B2018291 (1 mg)
Cholesteryl oleate-13C18 is a specific form of cholesteryl oleate where the carbon atoms in the molecule have been labeled with the stable isotope carbon-13. This labeling can be used in research and analytical studies to track the movement and metabolism of the molecule in biological systems. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

Cholesteryl oleate-13C18
Catalog number: B2018291
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 mg
Molecular Weight or Concentration: 668.97 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: -20°C
Keywords:
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Degirolamo C, Shelness GS, Rudel LL. LDL cholesteryl oleate as a predictor for atherosclerosis: evidence from human and animal studies on dietary fat J Lipid Res. 2009 Apr;50 Suppl(Suppl):S434-9.
2: Spector AA, Haynes WG. LDL cholesteryl oleate: a biomarker for atherosclerosis? Arterioscler Thromb Vasc Biol. 2007 Jun;27(6):1228-30.
3: Suñé-Pou M, Prieto-Sánchez S, El Yousfi Y, Boyero-Corral S, Nardi-Ricart A, Nofrerias-Roig I, Pérez-Lozano P, García-Montoya E, Miñarro-Carmona M, Ticó JR, Suñé-Negre JM, Hernández-Munain C, Suñé C. Cholesteryl oleate-loaded cationic solid lipid nanoparticles as carriers for efficient gene-silencing therapy Int J Nanomedicine. 2018 May 30;13:3223-3233.
4: Ishimoto A, Sasako H, Omori M, Higashi K, Ueda K, Koyama K, Moribe K. Drug-Loaded Nanocarriers Composed of Cholesteryl Oleate Crystal Cores and Multiple-Nanosheet Shells of γ-Cyclodextrin Inclusion Complex Crystals Langmuir. 2022 Aug 30;38(34):10454-10464.
5: Terpstra AH. Comparison of the metabolism of [1,2,6,7-3H(N)]cholesteryl oleate, cholesteryl [9,10-3H]oleate, and cholesteryl [1-14C]oleate labeled lipoproteins in the rat Atherosclerosis. 1994 Apr;106(2):203-11.
6: Suñé-Pou M, Limeres MJ, Nofrerias I, Nardi-Ricart A, Prieto-Sánchez S, El-Yousfi Y, Pérez-Lozano P, García-Montoya E, Miñarro-Carmona M, Ticó JR, Hernández-Munain C, Suñé C, Suñé-Negre JM. Improved synthesis and characterization of cholesteryl oleate-loaded cationic solid lipid nanoparticles with high transfection efficiency for gene therapy applications Colloids Surf B Biointerfaces. 2019 Aug 1;180:159-167.
7: Mims MP, Guyton JR, Morrisett JD. Microemulsions of cholesteryl oleate and dimyristoylphosphatidylcholine: a model for cholesteryl ester rich very low density lipoproteins Biochemistry. 1986 Jan 28;25(2):474-83.
8: Lee ES, Shon HK, Lee TG, Kim SH, Moon DW. The regional ratio of cholesteryl palmitate to cholesteryl oleate measured by ToF-SIMS as a key parameter of atherosclerosis Atherosclerosis. 2013 Feb;226(2):378-84.
9: Hamilton JA, Miller KW, Small DM. Solubilization of triolein and cholesteryl oleate in egg phosphatidylcholine vesicles J Biol Chem. 1983 Nov 10;258(21):12821-6.
10: Rudel LL, Haines J, Sawyer JK, Shah R, Wilson MS, Carr TP. Hepatic origin of cholesteryl oleate in coronary artery atherosclerosis in African green monkeys. Enrichment by dietary monounsaturated fat J Clin Invest. 1997 Jul 1;100(1):74-83.

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Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
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