Accéder au contenu
MilliporeSigma
Toutes les photos(3)

Key Documents

View All Documentation

840524P

Avanti

DGDG

Avanti Research™ - A Croda Brand

Synonyme(s) :

1,2-diacyl-3-O-(α-D-galactosyl1-6)-α-D-galactosyl-sn-glycerol

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(3)

About This Item

Numéro CAS:
63142-69-8
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Description

Digalactosyldiacylglycerol (Plant)

Pureté

>99% (TLC)

Forme

powder

Poids mol.

~926.77 g/mol (average based on fatty acid distribution)

Conditionnement

pkg of 1 × 5 mg (840524P-5mg)
pkg of 2 × 5 mg (840524P-10mg)
pkg of 5 × 5 mg (840524P-25mg)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand

Type de lipide

phosphoglycerides
bioactive lipids

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@](COC(CCCCCCC/C=C\C/C=C\C/C=C\CC)=O)(OC(CCCCCCC/C=C\C/C=C\C/C=C\CC)=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO[C@H](O2)[C@H](O)[C@@H](O)[C@H]([C@H]2CO)O)O

Description générale

Digalactosyldiacylglycerol (DGDG) is vital for photosynthesis.
Monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG) are the two nonionic lipid constituents of the thylakoid membrane of higher plant chloroplasts. MGDG and DGDG are present in the membrane at 56% and 29%, respectively, of the total lipid content. DGDG is a bilayer-forming lipid, while MGDG alone will only form hexagonal-II structures.

Application

Digalactosyldiacylglycerol (DGDG) has been used in hydrophilic interaction LC-ion mobility-MS (HILIC-IM-MS) for untargeted lipidomics.

Conditionnement

5 mL Amber Glass Screw Cap Vial (840524P-10mg)
5 mL Amber Glass Screw Cap Vial (840524P-25mg)
5 mL Amber Glass Screw Cap Vial (840524P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Souvent commandé avec ce produit

Réf. du produit
Description
Tarif

Code de la classe de stockage

11 - Combustible Solids

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".

Déjà en possession de ce produit ?

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

Consulter la Bibliothèque de documents

Reduced biosynthesis of digalactosyldiacylglycerol, a major chloroplast membrane lipid, leads to oxylipin overproduction and phloem cap lignification in Arabidopsis
Lin YT, et al.
Plant Cell, 28(1), 219-232 (2016)
Kuniyoshi Kaseda et al.
Pharmacological research, 152, 104633-104633 (2020-01-10)
Advanced glycation end products (AGEs) and their receptor (RAGE) system evoke inflammatory reactions and insulin resistance in adipocytes. Spa-derived green alga Mucidosphaerium sp. (MS) had anti-inflammatory properties in vitro. We examined here whether and how MS could ameliorate insulin resistance
Manuela Lenti et al.
Natural product research, 23(8), 754-762 (2009-05-07)
The mono- and the digalactosyldiacylglycerol (MGDG and DGDG) galactolipids with a high content of polyunsaturated fatty acids, mainly omega-3, have been purified from the thermophilic blue-green alga ETS-05 that colonises the therapeutic thermal mud of Abano and Montegrotto, Italy. The
Cyrille Y Botté et al.
The Journal of biological chemistry, 286(34), 29893-29903 (2011-06-30)
Apicomplexa are protist parasites that include Plasmodium spp., the causative agents of malaria, and Toxoplasma gondii, responsible for toxoplasmosis. Most Apicomplexa possess a relict plastid, the apicoplast, which was acquired by secondary endosymbiosis of a red alga. Despite being nonphotosynthetic
Characterization of the mechanisms of daptomycin resistance among Gram-positive bacterial pathogens by multidimensional lipidomics
Hines KM, et al.
mSphere, 2(6), e00492-e00417 (2017)
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique