810165P
Avanti
18:1-06:0 NBD PG
Avanti Research™ - A Croda Brand
Synonym(s):
1-oleoyl-2-{6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl}-sn-glycero-3-[phospho-rac-(1-glycerol)] (ammonium salt)
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About This Item
Empirical Formula (Hill Notation):
C36H62N5O13P
CAS Number:
Molecular Weight:
803.88
UNSPSC Code:
12352211
NACRES:
NA.25
Recommended Products
Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (810165P-1mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
shipped in
dry ice
storage temp.
−20°C
General description
Phosphatidylglycerol (PG) is an anionic phospholipid, constituting 20−25% in E. coli membranes. Nitrobenzoxadiazole phosphoglycerol (NBD PG) is a fluorescently labeled phospholipid with 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) attached to the fatty acid chain of the phosphatidylglycerol.
Application
18:1-06:0 NBD PG may be used in the determination of phosphatidylglycerol distribution across the bilayer of the membrane and to measure the rate constant for transbilayer movement of lipid molecules by preparing giant unilamellar vesicles (GUVs).
Biochem/physiol Actions
Phosphatidylglycerol is involved in the biosynthesis of cardiolipin. It also contributes to the photosynthetic activity by maintaining the structural photosynthetic apparatus.
Packaging
5 mL Amber Glass Screw Cap Vial (810165P-1mg)
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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Specificity of the transport of lipid II by FtsW in Escherichia coli
Mohammadi T, et al.
Journal of biological and chemical chronicles null
The role of membrane tension in the action of antimicrobial peptides and cell-penetrating peptides in biomembranes
Hasan M, et al.
Biophysical Reviews null
Phosphatidylglycerol is Essential for the Development of Thylakoid Membranes in Arabidopsis thaliana
Hagio M, et al.
Plant & Cell Physiology null
Helena Rosado et al.
International journal of molecular sciences, 16(8), 16710-16727 (2015-07-28)
The polyphenol (-)-epicatechin gallate (ECg) inserts into the cytoplasmic membrane (CM) of methicillin-resistant Staphylococcus aureus (MRSA) and reversibly abrogates resistance to β-lactam antibiotics. ECg elicits an increase in MRSA cell size and induces thickened cell walls. As ECg partially delocalizes
Tamimount Mohammadi et al.
The Journal of biological chemistry, 289(21), 14707-14718 (2014-04-09)
Synthesis of biogenic membranes requires transbilayer movement of lipid-linked sugar molecules. This biological process, which is fundamental in prokaryotic cells, remains as yet not clearly understood. In order to obtain insights into the molecular basis of its mode of action
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