1,2-dioctanoyl-sn-glycero-3-phosphocholine, 08:0 PC
<strong>1,2-dioctanoyl-sn-glycero-3-phosphocholine, 08:0 PC</strong>_x000D_ <strong>Catalog number:</strong> B2019241_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 10 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 509.614_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> 08:0 PC, PC(8:0/8:0)_x000D_ <strong>Grade:</strong> 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._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Davis LL, Maglio JJ, Horwitz J. Phospholipase D hydrolyzes short-chain analogs of phosphatidylcholine in the absence of detergent Lipids. 1998 Feb;33(2):223-7._x000D_ 2: Weinheimer M, Fricker G, Burhenne J, Mylius P, Schubert R. The application of P-gp inhibiting phospholipids as novel oral bioavailability enhancers - An in vitro and in vivo comparison Eur J Pharm Sci. 2017 Oct 15;108:13-22._x000D_ 3: Tanaka K, Fukuda R, Ono Y, Eguchi H, Nagasawa S, Nakatani Y, Watanabe H, Nakanishi H, Taguchi R, Ohta A. Incorporation and remodeling of extracellular phosphatidylcholine with short acyl residues in Saccharomyces cerevisiae Biochim Biophys Acta. 2008 Aug;1781(8):391-9._x000D_ 4: Palmerini T, Biondi-Zoccai G, Della Riva D, Stettler C, Sangiorgi D, D'Ascenzo F, Kimura T, Briguori C, Sabatè M, Kim HS, De Waha A, Kedhi E, Smits PC, Kaiser C, Sardella G, Marullo A, Kirtane AJ, Leon MB, Stone GW. Stent thrombosis with drug-eluting and bare-metal stents: evidence from a comprehensive network meta-analysis Lancet. 2012 Apr 14;379(9824):1393-402._x000D_ 5: Frostegård AG, Su J, Hua X, Vikström M, de Faire U, Frostegård J. Antibodies against native and oxidized cardiolipin and phosphatidylserine and phosphorylcholine in atherosclerosis development PLoS One. 2014 Dec 4;9(12):e111764._x000D_ 6: Fok TF, al-Essa M, Dolovich M, Rasid F, Kirpalani H. Nebulisation of surfactants in an animal model of neonatal respiratory distress Arch Dis Child Fetal Neonatal Ed. 1998 Jan;78(1):F3-9._x000D_ 7: Kansakar U, Trimarco V, Mone P, Varzideh F, Lombardi A, Santulli G. Choline supplements: An update Front Endocrinol (Lausanne). 2023 Mar 7;14:1148166._x000D_ 8: Kanda P, Wells MA. Synthesis of sn-glycero-1-phosphocholine J Lipid Res. 1981 Jul;22(5):879-82._x000D_ 9: Ładniak A, Jurak M, Wiącek AE. The effect of chitosan/TiO(2)/hyaluronic acid subphase on the behaviour of 1,2-dioleoyl-sn-glycero-3-phosphocholine membrane Biomater Adv. 2022 Jul;138:212934._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/38003442">10: Sudjarwo WAA, Toca-Herrera JL. Unraveling Complex Hysteresis Phenomenon in 1,2-Dipalmitoyl-sn-Glycero-3-Phosphocholine Monolayer: Insight into Factors Influencing Surface Dynamics Int J Mol Sci. 2023 Nov 13;24(22):16252. </a>_x000D_ _x000D_ <strong>Products Related to 1,2-dioctanoyl-sn-glycero-3-phosphocholine, 08:0 PC can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>
Product Specifications
Short Description
Catalog Number: B2019241 (10 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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