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Principaux documents

810153P

Avanti

16:0-06:0 NBD PE

Avanti Research - A Croda Brand 810153P, powder

Synonyme(s) :

1-palmitoyl-2-{6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl}-sn-glycero-3-phosphoethanolamine

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About This Item

Formule empirique (notation de Hill):
C33H56N5O11P
Numéro CAS:
Poids moléculaire :
729.80
Numéro MDL:
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Essai

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 1 mg (810153P-1mg)
pkg of 5 × 1 mg (810153P-5mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 810153P

Conditions d'expédition

dry ice

Température de stockage

−20°C

Description générale

N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) phosphoethanolamine (NBD PE) is a fluorescently labeled lipid localized at the membrane interface. The molecule contains NBD label covalently linked to the headgroup of phosphatidylethanolamine. PE is mostly present in the brain and is the second most abundant, metabolically related aminophospholipid.

Application

16:0-06:0 NBD PE is suitable for the determination of enzyme substrate specificity of lipoteichoic acid synthase (LtaS).

Actions biochimiques/physiologiques

N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) phosphoethanolamine (NBD PE) is involved in screening the effects of Red edge excitation shift (REES) experiment with the unique motional and dielectric property it possesses. PE functions as a substrate for a number of phospholipids of the cell membrane.

Conditionnement

5 mL Amber Glass Screw Cap Vial (810153P-1mg)
5 mL Amber Glass Screw Cap Vial (810153P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids


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Consulter la Bibliothèque de documents

Application of NBD-labeled lipids in membrane and cell biology
Fluorescent methods to study biological membranes, 37-50 (2012)
Adilson Kleber Ferreira et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 67(6), 481-487 (2013-06-19)
Phosphoethanolamine (Pho-s) is a compound involved in phospholipid turnover, acting as a substrate for many phospholipids of the cell membranes. In a recent study, we showed that Pho-s has antitumor effect in the several tumor cells. In this study we
Maria Mercedes Palomino et al.
Microbiology (Reading, England), 159(Pt 11), 2416-2426 (2013-09-10)
The probiotic Gram-positive bacterium Lactobacillus casei BL23 is naturally confronted with salt-stress habitats. It has been previously reported that growth in high-salt medium, containing 0.8 M NaCl, leads to modifications in the cell envelope of this bacterium. In this study
S C Lopes et al.
Biochimica et biophysica acta. Biomembranes, 1861(6), 1152-1161 (2019-03-07)
Mitochondrial membranes are pointed out as the site of cardiotoxic action of local anaesthetics. Its three main phospholipids components are phosphatidylcholine, phosphatidylethanolamine and cardiolipin. Cardiolipins, in eukaryotes, are only found in mitochondria and are essential for the maintenance of its
Jean E Vance et al.
Biochimica et biophysica acta, 1831(3), 543-554 (2012-09-11)
Phosphatidylserine (PS) and phosphatidylethanolamine (PE) are metabolically related membrane aminophospholipids. In mammalian cells, PS is required for targeting and function of several intracellular signaling proteins. Moreover, PS is asymmetrically distributed in the plasma membrane. Although PS is highly enriched in

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