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NBD-PE [N-(7-Nitrobenz-2-Oxa-1,3-Diazol-4-yl)-1,2-Dihexadecanoyl-sn-Glycero-3-Phosphoethanolamine, Triethylammonium Salt]

Product key features

  • Environment-Sensitive Fluorophore: NBD head group enables fluorescence changes based on membrane environment.
  • Optimal Spectral Properties: Ex/Em maxima at ~467/539 nm.
  • Membrane Integration: Efficiently incorporates into lipid bilayers for dynamic studies.
  • Versatile Applications: Ideal for studying membrane dynamics, fusion, and lipid interactions.

Product description

NBD-PE (N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)-1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine, triethylammonium salt) is a fluorescent phospholipid commonly used in cell biology research for studying membrane dynamics, including membrane fluidity and trafficking. Its ability to integrate seamlessly into cellular membranes and fluoresce upon excitation makes it a valuable tool for investigating the physical and functional properties of lipid bilayers.

This phospholipid is modified at its head group with the environment-sensitive fluorophore NBD, which has excitation and emission maxima at approximately 467 nm and 539 nm, respectively. When paired with complementary dyes such as Rhodamine-DHPE (#60026) or Texas Red®-DHPE (#60027), NBD-PE enables fluorescence resonance energy transfer (FRET)-based assays for studying membrane fusion events. Furthermore, it has been widely applied in fluorescence recovery after photobleaching (FRAP) experiments to quantitatively assess membrane dynamics and lipid mobility.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (280 nm)
NBD-F [4-Fluoro-7-nitrobenzofurazan] *CAS 29270-56-2*46753922000--
NBD-Cl [4-Chloro-7-nitrobenzofurazan] *CAS 10199-89-0*46753922000--
Phycoerythrin (PE)56557419600000.820.175
ReadiUse™ PE [R-Phycoerythrin] *Ammonium Sulfate-Free*56557419600000.820.175

References

View all 50 references: Citation Explorer
ATG9B is a tissue-specific homotrimeric lipid scramblase that can compensate for ATG9A.
Authors: Chiduza, George N and Garza-Garcia, Acely and Almacellas, Eugenia and De Tito, Stefano and Pye, Valerie E and van Vliet, Alexander R and Cherepanov, Peter and Tooze, Sharon A
Journal: Autophagy (2024): 557-576
Flow-based bioconjugation of coumarin phosphatidylethanolamine probes: Optimised synthesis and membrane molecular dynamics studies.
Authors: Varandas, Pedro A M M and Belinha, Ricardo and Cobb, Alexander J A and Prates Ramalho, João P and Segundo, Marcela A and Loura, Luís M S and Silva, Eduarda M P
Journal: Biochimica et biophysica acta. Biomembranes (2024): 184335
Fluorescent hydrophobic ion pairs: A powerful tool to investigate cellular uptake of hydrophobic drug complexes via lipid-based nanocarriers.
Authors: Zöller, Katrin and Karlegger, Anna and Truszkowska, Martyna and Stengel, Daniel and Bernkop-Schnürch, Andreas
Journal: Journal of colloid and interface science (2024): 174-188
--Atg9 interactions via its transmembrane domains are required for phagophore expansion during autophagy.
Authors: Chumpen Ramirez, Sabrina and Gómez-Sánchez, Rubén and Verlhac, Pauline and Hardenberg, Ralph and Margheritis, Eleonora and Cosentino, Katia and Reggiori, Fulvio and Ungermann, Christian
Journal: Autophagy (2023): 1459-1478
A Limitation of Using Dithionite Quenching to Determine the Topology of Membrane-inserted Proteins.
Authors: O'Neil, Pierce T
Journal: The Journal of membrane biology (2022): 123-127
Page updated on December 17, 2024

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Catalog Number23305
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Physical properties

Molecular weight

956.24

Solvent

DMSO

Spectral properties

Extinction coefficient (cm -1 M -1)

22000

Excitation (nm)

467

Emission (nm)

539

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure

CAS

178119-00-1
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