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810165P

Avanti

18:1-06:0 NBD PG

Avanti Polar Lipids

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

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 mg (810165P-1mg)

manufacturer/tradename

Avanti Polar Lipids

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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