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1,2-di-O-phytanyl-sn-glycero-3-phosphocholine (Highly Pure)

<strong>1,2-di-O-phytanyl-sn-glycero-3-phosphocholine (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2018526_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 818.284_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 PC_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Kim DT, Blanch HW, Radke CJ. Imaging of reconstituted purple membranes by atomic force microscopy Colloids Surf B Biointerfaces. 2005 Apr 10;41(4):263-76._x000D_ 2: Zeller J, Cheung Tung Shing KS, Nero TL, McFadyen JD, Krippner G, Bogner B, Kreuzaler S, Kiefer J, Horner VK, Braig D, Danish H, Baratchi S, Fricke M, Wang X, Kather MG, Kammerer B, Woollard KJ, Sharma P, Morton CJ, Pietersz G, Parker MW, Peter K, Eisenhardt SU. A novel phosphocholine-mimetic inhibits a pro-inflammatory conformational change in C-reactive protein EMBO Mol Med. 2023 Jan 11;15(1):e16236._x000D_ 3: Young NM, Foote SJ, Wakarchuk WW. Review of phosphocholine substituents on bacterial pathogen glycans: synthesis, structures and interactions with host proteins Mol Immunol. 2013 Dec;56(4):563-73._x000D_ 4: Kieber M, Ono T, Oliver RC, Nyenhuis SB, Tieleman DP, Columbus L. The Fluidity of Phosphocholine and Maltoside Micelles and the Effect of CHAPS Biophys J. 2019 May 7;116(9):1682-1691._x000D_ 5: Chipot C, Dehez F, Schnell JR, Zitzmann N, Pebay-Peyroula E, Catoire LJ, Miroux B, Kunji ERS, Veglia G, Cross TA, Schanda P. Perturbations of Native Membrane Protein Structure in Alkyl Phosphocholine Detergents: A Critical Assessment of NMR and Biophysical Studies Chem Rev. 2018 Apr 11;118(7):3559-3607._x000D_ 6: Xu LL, Berg LJ, Jamin Keith D, Townsend SD. An effective reagent to functionalize alcohols with phosphocholine Org Biomol Chem. 2020 Jan 28;18(4):767-770._x000D_ 7: Kim E, Lee SG, Kim HC, Lee SJ, Baek CS, Jeong SW. Protein-directed immobilization of phosphocholine ligands on a gold surface for multivalent C-reactive protein binding Curr Top Med Chem. 2013;13(4):519-24._x000D_ 8: Liu Y, Liu J. Adsorption of Nanoceria by Phosphocholine Liposomes Langmuir. 2016 Dec 13;32(49):13276-13283._x000D_ 9: Soto JA, Berman JD. Miltefosine Treatment of Cutaneous Leishmaniasis Clin Infect Dis. 2021 Oct 5;73(7):e2463-e2464._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/28471667">10: Frampton MB, Marquardt D, Letofsky-Papst I, Pabst G, Zelisko PM. Analysis of Trisiloxane Phosphocholine Bilayers Langmuir. 2017 May 23;33(20):4948-4953. </a>_x000D_ _x000D_ <strong>Products Related to 1,2-di-O-phytanyl-sn-glycero-3-phosphocholine (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>

Product Specifications

Short Description

Catalog Number: B2018526 (1 mg)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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