disialogangloside GD1a

disialogangloside GD1a - Names and Identifiers

Name	Ganglioside GD1A Disodium Salt
Synonyms	disialogangloside GD1a GANGLIOSIDE GD1A DISODIUM SALT Ganglioside GD1A Disodium Salt GANGLIOSIDEGD1ADISODIUMSALT,BOVINEBRAIN disialoganglioside-gd1A from bovinebrain ganglioside gd1a, disialo from bovine brain disialoganglioside G(D1A) from bovine brain DISIALOGANGLIOSIDE-GD1A CELL CULTURETES TED GANGLIOSIDEGD1ADISODIUMSALT,BOVINEBRAIN,CELLCULTUREGRADE Disialoganglioside GD1a from bovine brain,Ganglioside GD1a, disialo from bovine brain
CAS	12707-58-3

disialogangloside GD1a - Physico-chemical Properties

Molecular Formula	C84H146N4Na2O39
Molar Mass	1882.04098
Solubility	DMSO: soluble
Appearance	lyophilized powder
BRN	6228822
Storage Condition	-20°C

disialogangloside GD1a - Risk and Safety

Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
FLUKA BRAND F CODES	10-21
HS Code	29400090

disialogangloside GD1a - Introduction

Ganglioside GD1A Disodium Salt(Ganglioside GD1A Disodium Salt) is a lipid-like compound, which is a Ganglioside containing a diglycan sheath and an ester group. GD1A is an important bioactive molecule, which is widely present in the nervous tissue of mammals.

Regarding the nature of GD1A, it is a white or almost white powder, soluble in water. Under physiological conditions, GD1A can play an important role in cell membrane and participate in signal transduction and cell adhesion between nerve cells.

One of the main uses of GD1A is as an experimental tool for the Study of neurobiology and neurological function. It can be used to study the process of induced differentiation, migration, proliferation, survival and neurotransmitter release of neural cells. In addition, GD1A is used as an aid in the diagnosis and treatment of certain neurological disorders.

One way to produce GD1A is to extract and purify it from natural sources, such as animal nerve tissue. This process involves multiple steps of chemical treatment and chromatographic techniques. Alternatively, GD1A can be obtained by chemical synthesis, but this method is more complicated and expensive.

In terms of safety, GD1A is generally relatively safe under appropriate conditions of use. However, as a bioactive molecule, use and handling should follow relevant laboratory procedures and safety measures. In addition, direct contact with eyes, skin or inhalation of dust should be avoided, and appropriate personal protective equipment should be worn when necessary.

Last Update：2024-04-09 21:54:55