![]() 1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine, 7-nitrobenzofurazan-labeled structure
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Common Name | 1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine, 7-nitrobenzofurazan-labeled | ||
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CAS Number | 137819-86-4 | Molecular Weight | 907.12400 | |
Density | 1.115g/cm3 | Boiling Point | 891.9ºC at 760 mmHg | |
Molecular Formula | C47H79N4O11P | Melting Point | N/A | |
MSDS | USA | Flash Point | 493.2ºC |
Concentration dependence of lipopolymer self-diffusion in supported bilayer membranes.
J. R. Soc. Interface 8 , 127-143, (2011) Self-diffusion coefficients of poly(ethylene glycol)2k-derivatized lipids (DSPE-PEG2k-CF) in glass-supported DOPC phospholipid bilayers are ascertained from quantitative fluorescence recovery after photobleaching (FRAP). We developed a first-order reaction-di... |
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Biophysical characterization of complexes of DNA with mixtures of the neutral lipids 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-hexanoylamine or 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-dodecanoylamine and 1,2-dioleoyl-sn-glycero-3-phosphocholine in the presence of bivalent metal cations for DNA transfection.
J. Phys. Chem. B 115 , 10198-10296, (2011) Neutral lipids have received up to now a little attention as genetic material carriers, despite some valuable features, such as the absence of toxicity and the high stability in serum of their complexes with DNA. We have prepared two quaternary complexes of D... |
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Biophysical properties of ergosterol-enriched lipid rafts in yeast and tools for their study: characterization of ergosterol/phosphatidylcholine membranes with three fluorescent membrane probes.
Chem. Phys. Lipids 165 , 577-588, (2012) In this work, binary mixtures of phospholipid/ergosterol (erg) were studied using three fluorescent membrane probes. The phospholipid was either saturated (1,2-dipalmitoyl-sn-glycero-3-phosphocholine, DPPC) or monounsaturated (1-palmitoyl-2-dioleoyl-sn-glycer... |
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Ligand-based targeted delivery of a peptide modified nanocarrier to endothelial cells in adipose tissue. Hossen MN, Kajimoto K, Akita H, et al.
J. Controlled Release 147 , 261-268, (2010)
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