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810603C

Avanti

16:0-10 Doxyl PC

Avanti Research - A Croda Brand 810603C

Synonym(e):

1-palmitoyl-2-stearoyl-(10-doxyl)-sn-glycero-3-phosphocholine

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CHF 701.00

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CHF 701.00

About This Item

Empirische Formel (Hill-System):
C46H90N2O10P
CAS-Nummer:
Molekulargewicht:
862.19
MDL-Nummer:
UNSPSC-Code:
41141825
NACRES:
NA.12

CHF 701.00


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Assay

>99% (TLC)

Form

liquid

Verpackung

pkg of 1 × 1 mL (810603C-1mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 810603C

Konzentration

1 mg/mL (810603C-1mg)

Lipid-Typ

ESR probes
phospholipids

Versandbedingung

dry ice

Lagertemp.

−20°C

Allgemeine Beschreibung

Avanti′s nitroxide spin product listing is a group of compounds designed to act as membrane probes. A variety of positions down the hydrophobic chain are labeled with the nitroxide functional groups to allow probing the membrane at various depths. These compounds have been synthesized from 1-palmitoyl-2-hydroxy-sn-glycerol-3-phosphocholine with the product being purified by column chromatography. Various n-doxyl phosphocholines have been recently used as biophysical tools to elucidate membrane trafficking with phosphatidylinositol transfer proteins and as fluorescent quenchers in lipid bilayer structural studies.[1][2]
Phosphocholine is considered as a precursor molecule. It is formed during the breakdown of phosphatidylcholine metabolism.[3]

Anwendung

16:0-10 Doxyl PC may be used in vesicles for quenching PT-(1–46)F4W fluorescence.[4] It may also be used in vesicles to check the fluorescence emission spectra in order to measure the penetration depth of the peptides′ tryptophan residues in lipid bilayer.[5]

Biochem./physiol. Wirkung

Phosphatidylcholine (PC) lowers the levels of cholesterol and triglycerides.[6]

Verpackung

5 mL Clear Glass Sealed Ampule (810603C-1mg)

Angaben zur Herstellung

Product use: To prevent aggregation, prepare water-based solutions of 2 mM stock solutions of n-DOXYL PCs and store in plastic. Dilute stock solutions to 0.03- 0.1 mM solutions for EPR studies.[7] For liposome preparations in fluorescent quenching measurements, dissolve the doxyl lipid in 150 μl absolute ethanol for a concentration of 40.3 mM [2], Additional supplemental information.

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Piktogramme

Skull and crossbonesHealth hazard

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Zielorgane

Central nervous system, Liver,Kidney

WGK

WGK 3


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Die Dokumentenbibliothek aufrufen

Biology-cancer metabolic phenotype
NMR Metabolomics in Cancer Research, 15-138 (2013)
Q Wang et al.
Biochimica et biophysica acta, 1324(1), 69-75 (1997-02-21)
The N-terminal signal sequence of glucitol permease of Escherichia coli (Gut22: MIETITPGAVWFIGLFQKGGEC) and its analog (Gut22Ana: MIETITHGAEWFIGLFQKGGEC) were synthesized. The analog had a Pro residue substituted for the His at the 7th position of Gut22 and a Val residue substituted
L A Falls et al.
The Journal of biological chemistry, 276(26), 23895-23902 (2001-04-20)
The hydrophobic omega-loop within the prothrombin gamma-carboxyglutamic acid-rich (Gla) domain is important in membrane binding. The role of this region in membrane binding was investigated using a synthetic peptide, PT-(1-46)F4W, which includes the N-terminal 46 residues of human prothrombin with
Insight into antibody combining sites using nuclear magnetic resonance and spin label haptens
McConnell HM
Advances in Protein Chemistry, 49, 135-148 (1996)
Ultra-stable temperature control in EPR experiments: thermodynamics of gel-to-liquid phase transition in spin-labeled phospholipid bilayers and bilayer perturbations by spin labels
Alaouie AM, et. al.
Journal of Magnetic Resonance, 182, 229-238 (2006)

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