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Key Documents

860065P

Avanti

Ganglioside GM1 (Ovine Brain)

Avanti Research - A Croda Brand

Synonyme(s) :

110952

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About This Item

Numéro CAS:
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Description

GM1 Ganglioside (Brain, Ovine-Sodium Salt)

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 1 mg (860065P-1mg)
pkg of 1 × 10 mg (860065P-10mg)
pkg of 1 × 25 mg (860065P-25mg)
pkg of 1 × 5 mg (860065P-5mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand

Type de lipide

sphingolipids

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(CCCCCCCCCCCCCCCCC)=O)CO[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@@H]([C@H](O[C@@]3(C([O-])=O)O[C@@H]([C@H](O)[C@H](O)CO)[C@@](NC(C)=O)([H])[C@@H](O)C3)[C@H]2O)O[C@@H]4O[C@H](CO)[C@@H]([C@H](O[C@@H]5O[C@H

InChI

1S/C73H131N3O31/c1-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-52(86)76-44(45(83)33-31-29-27-25-23-21-18-16-14-12-10-8-6-2)40-99-69-61(93)59(91)63(50(38-79)102-69)104-71-62(94)67(98-41-47(85)55(87)66-53(74-42(3)81)46(84)35-73(97,107-66)72(95)96)64(51(39-80)103-71)105-68-54(75-43(4)82)65(57(89)49(37-78)100-68)106-70-60(92)58(90)56(88)48(36-77)101-70/h31,33,44-51,53-71,77-80,83-85,87-94,97H,5-30,32,34-41H2,1-4H3,(H,74,81)(H,75,82)(H,76,86)(H,95,96)/b33-31+/t44?,45?,46-,47?,48+,49+,50+,51+,53+,54+,55?,56-,57-,58-,59+,60+,61+,62+,63+,64-,65+,66+,67+,68-,69+,70-,71-,73-/m0/s1

Clé InChI

CNLVNZJJSHZYAS-ALSOZVJRSA-N

Description générale

Ganglioside GM1 is referred as brain ganglioside. It is an acidic glycosphingolipid comprising N-acetylneuraminic acid or N-glycolylneuraminic acid residues. It is upregulated in developing brain. Ganglioside GM1 has five glycosyl units.

Application

Ganglioside GM1 (Ovine Brain) has been used in the preparation of small unilamellar vesicles for fluorescence studies. It has also been used in liposome preparation for circular dichroism studies with human wild type−synuclein. It may be used as a standard lipid for electrospray ionization (ESI) mass spectrometry (MS) analysis.

Actions biochimiques/physiologiques

Ganglioside GM1 is a modulator of Ca2+ flux in plasmamembrane. It plays a key role in neuronal development and maturation and has neuroprotective functionality. GM1 ganglioside from ovine has many pharmaceutical applications and is regarded as an effective therapeutic for Huntington′s disease. Accumulation of GM1 in brain due to β-galactosidase enzyme deficiency is implicated in metabolic disorder, GM1 gangliosidosis.

Conditionnement

5 mL Amber Glass Screw Cap Vial (860065P-10mg)
5 mL Amber Glass Screw Cap Vial (860065P-1mg)
5 mL Amber Glass Screw Cap Vial (860065P-25mg)
5 mL Amber Glass Screw Cap Vial (860065P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

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)

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Consulter la Bibliothèque de documents

Formation of supported lipid bilayers containing phase-segregated domains and their interaction with gold nanoparticles
Melby ES, et al.
Environmental science : water research & technology, 3(1), 45-55 (2016)
Quantitative Comparison of GM1 Gangliosidosis Afflicted Ovine Tissue using Thin-Layer Chromatography, Mass Spectrometry and Nuclear Magnetic Resonance
Mata CV and Mitchell JC
Faseb Journal, 33(1), 796-715 (2019)
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis
De Grandis E, et al.
AJNR. American Journal of Neuroradiology, 30(7), 1325-1327 (2009)
Tyuji Hoshino et al.
The journal of physical chemistry. B, 117(27), 8085-8094 (2013-05-22)
Accumulation and fibril formation of amyloid β (Aβ) peptides onto a ganglioside-rich lipid membrane is a cause of neuro-disturbance diseases. To find out a measure for suppressing the nucleation of a seed for amyloid fibrils, the mechanism of the initial
The multi-tasked life of GM1 ganglioside, a true factotum of nature
Ledeen RW and Wu G
Trends in Biochemical Sciences, 40(7), 407-418 (2015)

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