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840857C

Avanti

16:0-18:1 PA

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt), chloroform

Synonym(e):

1-hexadecanoyl-2--(9Z-octadecenoyl)-sn-glycero-3-phosphate (sodium salt); POPA; PA(16:0/18:1(9Z)); 110616

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Empirische Formel (Hill-System):
C37H70O8PNa
CAS-Nummer:
Molekulargewicht:
696.91
UNSPSC-Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

Form

liquid

Verpackung

pkg of 1 × 2.5 mL (840857C-25mg)
pkg of 2 × 4 mL (840857C-200mg)
pkg of 5 × 4 mL (840857C-500mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 840857C

Konzentration

10 mg/mL (840857C-25mg)
25 mg/mL (840857C-200mg)
25 mg/mL (840857C-500mg)

Lipid-Typ

phospholipids
cardiolipins

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

[H][C@@](COP([O-])(O)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C37H71O8P.Na/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-37(39)45-35(34-44-46(40,41)42)33-43-36(38)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2;/h17-18,35H,3-16,19-34H2,1-2H3,(H2,40,41,42);/q;+1/p-1/b18-17-;/t35-;/m1./s1

InChIKey

PPYXMAJBOKWTQX-RYRMQHSSSA-M

Allgemeine Beschreibung

16:0-18:1 PA (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt)/POPA) has eight oxygen atoms and one hydroxyl hydrogen atom. POPA is an anionic lipid.

Anwendung

16:0-18:1 PA (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphate (sodium salt)) has been used to study its effects on the monogalactosyldiacylglycerol (MGDG) synthase activity of chloroplast envelope and in liposome Pull-Down Assay with the C2-like domain of SEIPIN.

Biochem./physiol. Wirkung

Phosphatidic acid (PA) serves as a precursor for phosphatidylcholine or phosphatidylserine. It is involved in influencing the membrane curvature and signaling.

Verpackung

5 mL Clear Glass Sealed Ampule (840857C-200mg)
5 mL Clear Glass Sealed Ampule (840857C-25mg)
5 mL Clear Glass Sealed Ampule (840857C-500mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

auch häufig zusammen mit diesem Produkt gekauft

Produkt-Nr.
Beschreibung
Preisangaben

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


Analysenzertifikate (COA)

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

Die Dokumentenbibliothek aufrufen

Allison Dickey et al.
Biophysical journal, 95(6), 2636-2646 (2008-06-03)
To better understand bilayer property dependency on lipid electrostatics and headgroup size, we use atomistic molecular dynamics simulations to study negatively charged and neutral lipid membranes. We compare the negatively charged phosphatidic acid (PA), which at physiological pH and salt
Nadezhda Y Davydova et al.
The Biochemical journal, 476(23), 3661-3685 (2019-11-22)
In this study, we investigate the ability of ethanol-inducible CYP2E1 to interact with other cytochrome P450 species and affect the metabolism of their substrates. As a model system, we used CYP2E1-enriched human liver microsomes (HLM) obtained by the incorporation of
Renhong Yan et al.
Developmental cell, 47(2), 248-256 (2018-10-09)
The biogenesis of lipid droplets (LDs) and the development of adipocytes are two key aspects of mammalian fat storage. SEIPIN, an integral membrane protein of the endoplasmic reticulum (ER), plays a critical role in both LD formation and adipogenesis. The
R J Perrin et al.
The Journal of biological chemistry, 275(44), 34393-34398 (2000-08-23)
alpha-Synuclein has been centrally implicated in neurodegenerative disease, and a normal function in developmental synaptic plasticity has been suggested by studies in songbirds. A variety of observations suggest the protein partitions between membrane and cytosol, a behavior apparently conferred by
Bixia Zhang et al.
Plant physiology (2020-04-26)
Cinnamate 4-hydroxylase (C4H, CYP73A) is a cytochrome P450 monooxygenase associated externally with endoplasmic reticulum of plant cells. The enzyme uses NADPH-cytochrome P450 reductase (CPR) as a donor of electrons and hydroxylates cinnamic acid to form 4-coumaric acid in phenylpropanoid metabolism.

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