1,2-Dipalmitoyl-sn-glycero-3-phosphocholine
Catalog Number: B2013603 (10 mg)
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine is a high quality 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine. This product has been used as 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.
Live enquiry about this product via Text/SMS: 1-858-900-3210.
Product Description
1,2-Dipalmitoyl-sn-glycero-3-phosphocholine
Catalog number: B2013603
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 mg
Molecular Weight or Concentration: N/A
Supplied as: Neat
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine
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: Zaytseva YV, Surovtsev NV. Raman scattering in protonated and deuterated 1,2-dipalmitoyl-sn-glycero-3_phosphatidylcholine (DPPC): Indicators of conformational and lateral orders Spectrochim Acta A Mol Biomol Spectrosc. 2022 Feb 15;267(Pt 2):120583.
2: Chen D, Santore MM. 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC)-rich domain formation in binary phospholipid vesicle membranes: two-dimensional nucleation and growth Langmuir. 2014 Aug 12;30(31):9484-93.
3: Brimble PD, Choy PC. Synthesis of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine with labeled acyl groups Prep Biochem. 1981;11(5):525-33.
4: Aikawa T, Sato K, Okado H, Takahashi Y, Kondo T, Yuasa M. Lyoprotective Effect of Alkyl Sulfobetaines for Freeze-drying 1,2-Dipalmitoyl-sn-glycero_3-phosphocholine Liposomes J Oleo Sci. 2017 Nov 1;66(11):1277-1284.
5: Pares-Lara A, Ausili A, Aranda FJ, de Godos A, Torrecillas A, Corban-Garcia S, G0mez-Fern¡ndez JC. Curcumin disorders 1,2-dipalmitoyl-sn-glycero-3-phosphocholine membranes and favors the formation of nonlamellar structures by 1,2-dielaidoyl-sn-glycero-3-phosphoethanolamine J Phys Chem B. 2010 Aug 5;114(30):9778-86.
6: Joondan N, Jhaumeer-Laulloo S, Caumul P. A study of the antibacterial activity of L-phenylalanine and L-tyrosine esters in relation to their CMCs and their interactions with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, DPPC as model membrane Microbiol Res. 2014 Sep-Oct;169(9-10):675-85.
7: Joondan N, Caumul P, Akerman M, Jhaumeer-Laulloo S. Synthesis, micellisation and interaction of novel quaternary ammonium compounds derived from l-Phenylalanine with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine as model membrane in relation to their antibacterial activity, and their selectivity over human red blood cells Bioorg Chem. 2015 Feb;58:117-29.
8: Scissor A, Koglin E, Meier RJ, Klumpp E. The phase transition behavior of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) model membrane influenced by 2,4-dichlorophenol–an FT-Raman spectroscopy study Chem Phys Lipids. 2006 Feb;139(2):115-24.
9: Umemura J, Cameron DG, Mantsch HH. A Fourier transform infrared spectroscopic study of the molecular interaction of cholesterol with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine Biochim Biophys Acta. 1980 Oct 16;602(1):32-44.
10: Yamauchi K, Togawa K, Kinoshita M. Synthesis and properties of dimeric glycerophospholipid: 2,2′-dotriacontanedioylbis(1-palmitoyl-sn-glycero-3-phosphocholine) J Biochem. 1996 Jan;119(1):115-9.
Products Related to 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine can be found at Lipids
Additional Information
| Weight | 48 oz |
|---|---|
| Dimensions | 8 × 8 × 8 in |