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810123P

Avanti

14:0-12:0 NBD PC

Avanti Research - A Croda Brand 810123P, powder

Synonym(e):

1-Myristoyl-2-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-sn-Glycero-3-Phosphocholine

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About This Item

Empirische Formel (Hill-System):
C40H70N5O11P
CAS-Nummer:
Molekulargewicht:
827.98
UNSPSC-Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

Form

powder

Verpackung

pkg of 1 × 1 mg (810123P-1mg)
pkg of 5 × 2 mg (810123P-10mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 810123P

Lipid-Typ

fluorescent lipids
phospholipids

Versandbedingung

dry ice

Lagertemp.

−20°C

Verwandte Kategorien

Allgemeine Beschreibung

Phosphatidylcholine (PC) is the most abundant phospholipid in eukaryotes. It is the prime metabolite of glycerolipid metabolism and a vital component of the mucosal layer of the colon. NBD PC has 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) moiety attached to phosphatidylcholine.

Anwendung

14:0-12:0 NBD PC has been used to prepare fluorescently labeled 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) unilamellar vesicles (LUVs) for the measurement lipid mass distribution. It may also be used to determine in vitro Phospholipase D (PLD) activity.

Biochem./physiol. Wirkung

7-nitrobenz-2-oxa-1,3-diazol-4-yl phosphatidylcholine (NBD PC) functions as fluorescent probe involved in the study of the biological membranes in cellular processes. It is a strong bilayer-forming lipid.

Verpackung

5 mL Amber Glass Screw Cap Vial (810123P-10mg)
5 mL Amber Glass Screw Cap Vial (810123P-1mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Takeshi Yamaguchi et al.
Plant physiology, 150(1), 308-319 (2009-03-17)
Phospholipase D (PLD) plays an important role in plants, including responses to abiotic as well as biotic stresses. A survey of the rice (Oryza sativa) genome database indicated the presence of 17 PLD genes in the genome, among which OsPLDalpha1
Eric Oropeza-Guzman et al.
Langmuir : the ACS journal of surfaces and colloids, 35(50), 16528-16535 (2019-11-21)
We took advantage of the microflow hydrodynamics in the evaporation of sessile droplets to increase the height uniformity of thin lipid films for the subsequent electroformation of defect-free giant unilamellar vesicles (GUV). By serially casting progressively larger liposome suspension droplets
Luís M S Loura et al.
Biochimica et biophysica acta, 1778(2), 491-501 (2007-11-21)
We present a combined theoretical (molecular dynamics, MD) and experimental (differential scanning calorimetry, DSC) study of the effect of 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) acyl chain-labeled fluorescent phospholipid analogs (C6-NBD-PC and C12-NBD-PC) on 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers. DSC measurements reveal that <1 mol% of
César Botella et al.
Progress in lipid research, 65, 12-23 (2016-11-23)
In plant cells, phosphatidylcholine (PC) is a major glycerolipid of most membranes but practically lacking from the plastid internal membranes. In chloroplasts, PC is absent from the thylakoids and the inner envelope membrane. It is however the main component of
Jelske N van der Veen et al.
Biochimica et biophysica acta. Biomembranes, 1859(9 Pt B), 1558-1572 (2017-04-16)
Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) are the most abundant phospholipids in all mammalian cell membranes. In the 1950s, Eugene Kennedy and co-workers performed groundbreaking research that established the general outline of many of the pathways of phospholipid biosynthesis. In recent

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