Direkt zum Inhalt
Merck

860345P

Avanti

14:0 PC-d54

1,2-dimyristoyl-d54-sn-glycero-3-phosphocholine, powder

Synonym(e):

DMPC-D54

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise

Größe auswählen

10 MG
142,00 €
25 MG
251,00 €
100 MG
671,00 €
200 MG
1.010,00 €

142,00 €


Auf LagerDetails


Bulk-Bestellung anfordern

Größe auswählen

Ansicht ändern
10 MG
142,00 €
25 MG
251,00 €
100 MG
671,00 €
200 MG
1.010,00 €

About This Item

Empirische Formel (Hill-System):
C36H18NO8PD54
CAS-Nummer:
Molekulargewicht:
732.27
MDL-Nummer:
UNSPSC-Code:
51191904
NACRES:
NA.25

142,00 €


Auf LagerDetails


Bulk-Bestellung anfordern

Assay

>99% (TLC)

Form

powder

Verpackung

pkg of 1 × 10 mg (860345P-10mg)
pkg of 1 × 100 mg (860345P-100mg)
pkg of 1 × 200 mg (860345P-200mg)
pkg of 1 × 25 mg (860345P-25mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 860345P

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)COC(C([2H])([2H])C([2H])([2H])C([2H])([2H

InChI

1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1/i1D3,2D3,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2,18D2,19D2,20D2,21D2,22D2,23D2,24D2,25D2,26D2,27D2,28D2,29D2

InChIKey

CITHEXJVPOWHKC-RPLUSTTMSA-N

Allgemeine Beschreibung

Deuterated fatty acids experience exchange of the deuteriums on the alpha carbon to the carbonyl, i.e., C2 position, and will therefore be a mixture of compounds that are fully deuterated and partially deuterated at that position.
Phosphocholine is a metabolic intermediate of phosphatidylcholine synthesis. Phosphorylation of choline in the presence of ATP yield phosphocholine.[1]

Anwendung

14:0 PC-d54 is suitable to reconstitute [ILV-13CH3, U-15N, 2H] labeled EmrE in n-dodecyl-β-D-maltopyranoside (DDM) back-exchanged to 1H at the amide positions during nuclear magnetic resonance (NMR) sample preparation.[2] It is also suitable for the preparation of phospholipid liposomes.[3]

Verpackung

5 mL Amber Glass Screw Cap Vial (860345P-100mg)
5 mL Amber Glass Screw Cap Vial (860345P-10mg)
5 mL Amber Glass Screw Cap Vial (860345P-200mg)
5 mL Amber Glass Screw Cap Vial (860345P-25mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

auch häufig zusammen mit diesem Produkt gekauft

Produkt-Nr.
Beschreibung
Preisangaben

Lagerklassenschlüssel

11 - Combustible Solids


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Dokumente section.

Wenn Sie Hilfe benötigen, wenden Sie sich bitte an Kundensupport

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Alessio Ausili et al.
Langmuir : the ACS journal of surfaces and colloids, 36(4), 1062-1073 (2020-01-14)
Vitamin K1 and vitamin K2 play very important biological roles as members of chains of electron transport as antioxidants in membranes and as cofactors for the posttranslational modification of proteins that participate in a number of physiological functions such as
Protonation of a glutamate residue modulates the dynamics of the drug transporter EmrE
Gayen A, et al.
Nature chemical biology, 12(3), 141-141 (2016)
Fusion of Legionella pneumophila outer membrane vesicles with eukaryotic membrane systems is a mechanism to deliver pathogen factors to host cell membranes
Jager J, et al.
Cellular Microbiology, 17(5), 607-620 (2015)
Phosphatidylcholine and the CDP-Choline Cycle
Fagone P, et al.
Biochimica et Biophysica Acta, 1831(5) (2013)
Jess Li et al.
The Journal of biological chemistry, 295(9), 2664-2675 (2020-01-25)
Engineering and bioconjugation of proteins is a critically valuable tool that can facilitate a wide range of biophysical and structural studies. The ability to orthogonally tag or label a domain within a multidomain protein may be complicated by undesirable side

Artikel

The critical micelle concentration (CMC) can be approximately defined as the lipid monomer concentration at which appreciable amounts (>5% of total) of micellar aggregates first begin to appear in the equilibrium: nM1<=>Mn

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.