810528P
Avanti
16:0 DNP Cap PE
1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[6-[(2,4-dinitrophenyl)amino]hexanoyl] (ammonium salt), powder
Synonym(s):
1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine-N-[6-[(2,4-dinitrophenyl)amino]caproyl] (ammonium salt)
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About This Item
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Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 25 mg (810528P-25mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 810528P
shipped in
dry ice
storage temp.
−20°C
General description
Phosphoethanolamine is a precursor to phosphatidylcholine and phosphatidylethanolamine. 2,4-dinitrophenol (DNP) is a synthetic lipid-soluble compound which transports ions across the bioenergetic membranes.
Application
16:0 DNP Cap PE may be used in Rho-PE-doped ink solution for the cell recruiting based lipid array experiments.
Biochem/physiol Actions
Phosphoethanolamine participates in phospholipid metabolism. It has the ability to repress tumor growth both in vitro and in vivo.
Packaging
5 mL Clear Glass Sealed Ampule (810528P-25mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
Certificates of Analysis (COA)
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Fumonisin, Folate, and Neural Tube Defects
Comprehensive Toxicology, 12, 189-208 (2010)
Membrane Transport
An Introduction to Biological Membranes, 423-451 (2016)
The Analyst, 137(13), 3076-3082 (2012-05-26)
The present work demonstrates for the first time patterning of a ready-to-use biosensor with several different biomolecules using Dip-Pen Nanolithography (DPN) for the development of a procedure towards more rapid and efficient multi-sample detection. The biosensor platform used is based
Polymers, 11(5) (2019-05-18)
Lipid-based membranes play crucial roles in regulating the interface between cells and their external environment, the communication within cells, and cellular sensing. To study these important processes, various lipid-based artificial membrane models have been developed in recent years and, indeed
Brain research, 417(2), 389-392 (1987-08-11)
Measurements of both phosphoethanolamine (PEA) and ethanolamine (EA) were made in postmortem brain samples from patients with Alzheimer's disease (AD) and Huntington's disease (HD) using high-performance liquid chromatography with electrochemical detection. In AD levels of PEA were significantly reduced by
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