1,2-di-O-phytanyl-sn-glycero-3-phosphoethanolamine (Highly Pure)
<strong>1,2-di-O-phytanyl-sn-glycero-3-phosphoethanolamine (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2018533_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> 776.205_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> 4ME 16:0 Diether PE_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: Kohli N, Hassler BL, Parthasarathy L, Richardson RJ, Ofoli RY, Worden RM, Lee I. Tethered lipid bilayers on electrolessly deposited gold for bioelectronic applications Biomacromolecules. 2006 Dec;7(12):3327-35._x000D_ 2: Fezza F, Mastrangelo N, Maccarrone M. Radiometric Assay of NAPE-PLD Activity Methods Mol Biol. 2023;2576:225-232._x000D_ 3: Zhou L, Zhao M, Bindler F, Marchioni E. Identification of Oxidation Compounds of 1-Stearoyl-2-linoleoyl-sn-glycero-3-phosphoethanolamine during Thermal Oxidation J Agric Food Chem. 2015 Nov 4;63(43):9615-20._x000D_ 4: Tian S, Ohtsuka J, Wang S, Nagata K, Tanokura M, Ohta A, Horiuchi H, Fukuda R. Human CTP:phosphoethanolamine cytidylyltransferase: enzymatic properties and unequal catalytic roles of CTP-binding motifs in two cytidylyltransferase domains Biochem Biophys Res Commun. 2014 Jun 20;449(1):26-31._x000D_ 5: Patel D, Witt SN. Ethanolamine and Phosphatidylethanolamine: Partners in Health and Disease Oxid Med Cell Longev. 2017;2017:4829180._x000D_ 6: KOPPEL JL, MUELLER DA, NOVAK LV, OLWIN JH. Effects of phosphoethanolamine and phosphoserine on blood coagulation mechanism Am J Physiol. 1959 May;196(5):1020-4._x000D_ 7: Hu K, Zhang Q, Chen Y, Yang J, Xia Y, Rao B, Li S, Shen Y, Cao M, Lu H, Qin A, Jiang XC, Yao D, Zhao J, Zhou L, Cao Y. Cryo-EM structure of human sphingomyelin synthase and its mechanistic implications for sphingomyelin synthesis Nat Struct Mol Biol. 2024 Jun;31(6):884-895._x000D_ 8: Kano-Sueoka T, Errick JE. Effects of phosphoethanolamine and ethanolamine on growth of mammary carcinoma cells in culture Exp Cell Res. 1981 Nov;136(1):137-45._x000D_ 9: Malgat M, Maurice A, Baraud J. Sphingomyelin and ceramide-phosphoethanolamine synthesis by microsomes and plasma membranes from rat liver and brain J Lipid Res. 1986 Mar;27(3):251-60._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/25846400">10: Nowicki EM, O'Brien JP, Brodbelt JS, Trent MS. Extracellular zinc induces phosphoethanolamine addition to Pseudomonas aeruginosa lipid A via the ColRS two-component system Mol Microbiol. 2015 Jul;97(1):166-78. </a>_x000D_ _x000D_ <strong>Products Related to 1,2-di-O-phytanyl-sn-glycero-3-phosphoethanolamine (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>
Product Specifications
Short Description
Catalog Number: B2018533 (10 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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