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840475C

Avanti

18:1 (Δ9-Cis) PG

Avanti Research - A Croda Brand

Synonyme(s) :

1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phospho-(1′racglycerol) (sodium salt); DOPG; PG(18:1(9Z)/18:1(9Z))

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About This Item

Formule empirique (notation de Hill):
C42H78O10PNa
Numéro CAS:
Poids moléculaire :
797.03
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Description

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

Pureté

>99% (TLC)

Forme

liquid

Conditionnement

pkg of 1 × 2.5 mL (840475C-25mg)
pkg of 2 × 4 mL (840475C-200mg)
pkg of 5 × 4 mL (840475C-500mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand

Concentration

10 mg/mL (840475C-25mg)
25 mg/mL (840475C-200mg)
25 mg/mL (840475C-500mg)

Type de lipide

cardiolipins
phospholipids

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

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

Catégories apparentées

Description générale

Phosphoglyceride (PG) are also referred as glycerophospholipid. It is an important component of membrane bilayers. It has three-carbon backbone of glycerol, two long-chain fatty acids, esterified to hydroxyl groups on carbons 1 and 2 of the glycerol and phosphoric acid esterified to the C3 hydroxyl group of glycerol. It is found at high levels in the membranes of all cells and at low levels in fat stores. 1,2-dioleoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (DOPG)/18:1 (Δ9-Cis) PG has two hydroxyl groups in its head group. It is an anionic lipid.

Application


  • Probing the extended lipid anchorage with cytochrome c and liposomes containing diacylphosphatidylglycerol lipids.: This study investigates the interactions of cytochrome c with liposomes containing diacylphosphatidylglycerol (PG) lipids, including 18:1 (Δ9-Cis) PG. The research provides insights into the lipid anchorage and membrane dynamics, which are crucial for understanding cellular processes and developing biotechnological applications involving lipid-protein interactions (Abbott et al., 2018).

Actions biochimiques/physiologiques

Phosphoglycerides (PG)/glycerophospholipids play a key role in cell signaling systems. It also serves as an anchor for proteins in cell membranes.

Conditionnement

5 mL Clear Glass Sealed Ampule (840475C-200mg)
5 mL Clear Glass Sealed Ampule (840475C-25mg)
5 mL Clear Glass Sealed Ampule (840475C-500mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system, Liver,Kidney

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Lipids
Medical Biochemistry, 99- 119 (2017)
Membrane Structure and Dynamics
Cell Biology, 227- 239 (2017)
Md Zahidul Islam et al.
Langmuir : the ACS journal of surfaces and colloids, 33(9), 2433-2443 (2017-02-07)
The translocation of cell-penetrating peptides (CPPs) through plasma membranes of living cells is an important physiological phenomenon in biomembranes. To reveal the mechanism underlying the translocation of a CPP, transportan 10 (TP10), through lipid bilayers, we examined the effects of
Mariya Chavarha et al.
Biophysical journal, 104(3), 594-603 (2013-02-28)
The hydrophobic surfactant proteins, SP-B and SP-C, greatly accelerate the adsorption of the surfactant lipids to an air/water interface. Previous studies of factors that affect curvature suggest that vesicles may adsorb via a rate-limiting structure with prominent negative curvature, in
Alexandre M Almeida et al.
Langmuir : the ACS journal of surfaces and colloids, 35(51), 16745-16751 (2019-11-21)
The alarming increase in bacterial resistance to antibiotics has demanded new strategies for microbial inactivation, which include photodynamic therapy whose activity relies on the photoreaction damage to the microorganism membrane. Herein, the binding mechanisms of the photosensitizer toluidine blue-O (TBO)

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