NBD-PE

For research use only. Not for therapeutic Use.

  • CAT Number: R072062
  • CAS Number: 178119-00-1
  • Molecular Formula: C49H90N5O11P
  • Molecular Weight: 956.24
  • Purity: ≥95%
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NBD-PE is an effective lipid fluorescent probe (Excitation/Emission: 465/535 nm; Color: Green). NBD-PE offers a wide array of applications in membrane and cell biology[1][2][3].
Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).
Assay of phospholipid transfer activity[3]:
1. The reaction mixture containes 2 mg mitochondrial protein, 0.02 μmol of NBD-PE, 0.5 mmol of Tris-HCl, pH 7.4, and 0-200 μg of pH 5.l-supernatant protein.
2. Samples are incubated at 37°C for 1 hour with gentle agitation.
3. The reaction is terminated by placing samples in an ice bath for 10 min, followed by centrifugation at 15,000 g for 5 min.
4. The supernatants are decanted, allowed to come to room temperature, and the absorbance (460 nm) and the relative fluorescence at 535 nm (excitation at 465 nm) are determined.
5. Blanks containing only NBD-PE and exchange protein are run concomitantly to correct for possible interaction between NBD-PE and exchange protein.
6. The percent exchange of NBD-PE is calculated from the differences between the absorbances or relative fluorescence in the supernatant fractions in the presence and absence of exchange protein.


Catalog Number R072062
CAS Number 178119-00-1
Synonyms

N,N-diethylethanamine;[(2R)-2-hexadecanoyloxy-3-[hydroxy-[2-[(4-nitro-2,1,3-benzoxadiazol-7-yl)amino]ethoxy]phosphoryl]oxypropyl] hexadecanoate

Molecular Formula C49H90N5O11P
Purity ≥95%
InChI InChI=1S/C43H75N4O11P.C6H15N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-40(48)54-35-37(57-41(49)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)36-56-59(52,53)55-34-33-44-38-31-32-39(47(50)51)43-42(38)45-58-46-43;1-4-7(5-2)6-3/h31-32,37,44H,3-30,33-36H2,1-2H3,(H,52,53);4-6H2,1-3H3/t37-;/m1./s1
InChIKey LEJHDNAGUHKMLR-GKEJWYBXSA-N
SMILES CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCCNC1=CC=C(C2=NON=C12)[N+](=O)[O-])OC(=O)CCCCCCCCCCCCCCC.CCN(CC)CC
Reference

[1]. M Esfahani, et al. 19F-NMR and fluorescence polarization of yeast plasma membrane and isolated lipids. Biochem Biophys Res Commun. 1981 Jul 16;101(1):306-11.
 [Content Brief]

[2]. P S Uster, et al. Resonance energy transfer microscopy: visual colocalization of fluorescent lipid probes in liposomes. Methods Enzymol. 1989;171:850-7.
 [Content Brief]

[3]. J A Monti, et al. Synthesis and properties of a highly fluorescent derivative of phosphatidylethanolamine. J Lipid Res. 1978 Feb;19(2):222-8.
 [Content Brief]

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