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850404C

Avanti

4ME 16:0 PG

1,2-diphytanoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt), chloroform

Synonym(e):

1,2-di-(3,7,11,15-tetramethylhexadecanoyl)-sn-glycero-3-phospho-(1′racglycerol) (sodium salt); PG(16:0(3me,7me,11me,15me)/16:0(3me,7me,11me,15me))

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About This Item

Empirische Formel (Hill-System):
C46H90O10PNa
CAS-Nummer:
474967-73-2
Molekulargewicht:
857.16
MDL-Nummer:
MFCD00674319
UNSPSC-Code:
12352211
NACRES:
NA.25

CHF 212.00

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Assay

>99% (TLC)

Form

liquid

Verpackung

pkg of 1 × 2.5 mL (850404C-25mg)

Hersteller/Markenname

Avanti Research™ - A Croda Brand 850404C

Konzentration

10 mg/mL (850404C-25mg)

Versandbedingung

dry ice

Lagertemp.

−20°C

Allgemeine Beschreibung

4ME 16:0 PG (DPhPG/1,2-diphytanoyl-sn-glycero-3-phospho-(1′-rac-glycerol)) is a negatively charged phospholipid. It has 16-carbon long hydrocarbon chains that are methyl-branched.[1] It is a fatty acid modified lipid.

Anwendung

4ME 16:0 PG (DPhPG/1,2-diphytanoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (sodium salt)) may be used:
  • as a phospholipid standard to quantify phosphatidylglycerol in plant samples by mass spectrometry analysis[2]
  • as a component of giant unilamellar vesicles (GUVs)for electrophysiology studies[3]
  • in the preparation of DPhPC (1,2-diphytanoyl-sn-glycero-3-phosphocholine/DPhPG vesicles[4]

Biochem./physiol. Wirkung

DPhPG/1,2-diphytanoyl-sn-glycero-3-phospho-(1′-rac-glycerol) is used in electrophysiological experiments.[5]

Verpackung

5 mL Clear Glass Sealed Ampule (850404C-25mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

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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Lot/Batch Number

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Extraction and profiling of plant polar glycerol lipids
Liu Y and Wang X
Bio-protocol, 6, 1849e-1849e null
Max Lein et al.
Biochimica et biophysica acta, 1848(11 Pt A), 2980-2984 (2015-09-08)
The mechanism(s) by which certain small peptides and peptide mimics carry large cargoes across membranes through exclusively non-covalent interactions has been difficult to resolve. Here, we use the droplet-interface bilayer as a platform to characterize distinct mechanistic differences between two
Giorgia Manzo et al.
Scientific reports, 9(1), 10934-10934 (2019-07-31)
Frogs such as Rana temporaria and Litoria aurea secrete numerous closely related antimicrobial peptides (AMPs) as an effective chemical dermal defence. Damage or penetration of the bacterial plasma membrane is considered essential for AMP activity and such properties are commonly
Hanieh Niroomand et al.
Scientific reports, 7(1), 2492-2492 (2017-06-01)
The role of natural thylakoid membrane housing of Photosystem I (PSI), the transmembrane photosynthetic protein, in its robust photoactivated charge separation with near unity quantum efficiency is not fundamentally understood. To this end, incorporation of suitable protein scaffolds for PSI
Sezgin Kara et al.
Biochimica et biophysica acta. Biomembranes, 1859(10), 1828-1837 (2017-06-08)
The branched chains in diphytanoyl lipids provide membranes with unique properties, such as high chemical/physical stability, low water permeability, and no gel-to-fluid phase transition at ambient temperature. Synthetic diphytanoyl phospholipids are often used as model membranes for electrophysiological experiments. To
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