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Citations & References (10)
Invitrogen™
BODIPY™ FL DHPE (N-(4,4-Difluoro-5,7-Dimethyl-4-Bora-3a,4a-Diaza-s-Indacene-3-Propionyl)-1,2-Dihexadecanoyl-sn-Glycero-3-Phosphoethanolamine, Triethylammonium Salt)
BODIPY™ DHPE has the green-fluorescent dye attached to the head group of the phospholipid. BODIPY™ FL can form excimers atRead more
| Catalog Number | Quantity |
|---|---|
| D3800 | 100 μg |
Catalog number D3800
Price (CNY)
2,732.00
Online Exclusive
Ends: 31-Dec-2025
3,704.00Save 972.00 (26%)
Each
Quantity:
100 μg
Price (CNY)
2,732.00
Online Exclusive
Ends: 31-Dec-2025
3,704.00Save 972.00 (26%)
Each
BODIPY™ DHPE has the green-fluorescent dye attached to the head group of the phospholipid. BODIPY™ FL can form excimers at high concentrations and unlike fluorophores like pyrene, DPH and NBD, BODIPY™ FL is relatively environment insensitive and is fluorescent in both aqueous and lipid environments.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical Name or MaterialPhospholipids
Recommended StorageStore in freezer (-5 to -30°C) and protect from light.
Physical FormSolid
Product LineBODIPY
Quantity100 μg
Unit SizeEach
Citations & References (10)
Citations & References
Abstract
Cell-free reconstitution of vacuole membrane fragmentation reveals regulation of vacuole size and number by TORC1.
Journal:Mol Biol Cell
PubMed ID:22238359
'Size and copy number of organelles are influenced by an equilibrium of membrane fusion and fission. We studied this equilibrium on vacuoles-the lysosomes of yeast. Vacuole fusion can readily be reconstituted and quantified in vitro, but it had not been possible to study fission of the organelle in a similar
Novel Fusogenic Liposomes for Fluorescent Cell Labeling and Membrane Modification.
Journal:Bioconjug Chem
PubMed ID:20184308
'Efficient delivery of biomolecules into membranes of living cells as well as cell surface modifications are major biotechnological challenges. Here, novel liposome systems based on neutral and cationic lipids in combination with lipids modified by aromatic groups are introduced for such applications. The fusion efficiency of these liposome systems was
Group V phospholipase A2 induces leukotriene biosynthesis in human neutrophils through the activation of group IVA phospholipase A2.
Journal:J Biol Chem
PubMed ID:12124392
'We reported previously that exogenously added human group V phospholipase A(2) (hVPLA(2)) could elicit leukotriene B(4) (LTB(4)) biosynthesis in human neutrophils (Han, S. K., Kim, K. P., Koduri, R., Bittova, L., Munoz, N. M., Leff, A. R., Wilton, D. C., Gelb, M. H., and Cho, W. (1999) J. Biol. Chem.
Determination of the depth of BODIPY probes in model membranes by parallax analysis of fluorescence quenching.
Journal:Biochim Biophys Acta
PubMed ID:9767081
'The location of a series of lipophilic and lipid-attached BODIPY (4, 4-difluoro-4-bora-3a,4a-diaza-s-indacene) membrane probes was analyzed by the quenching of BODIPY fluorescence by a series of nitroxide-labeled lipids in which the depth of the nitroxide group is varied. When attached to the polar headgroup of PE the BODIPY remained near
The antimicrobial peptide trichogin and its interaction with phospholipid membranes.
Journal:Eur J Biochem
PubMed ID:10583397
'The interaction of the antimicrobial peptide trichogin GA IV with phospholipid bilayers has been studied. A series of analogs of trichogin was synthesized in which the nitroxide spin label, 4-amino-4-carboxy-2,2,6,6-tetramethylpiperidino-1-oxyl (TOAC), replaced one of the three alpha-aminoisobutyric acid (Aib) residues in the sequence. These modified peptides were used to assess