您的位置:首页>>分析化学>>脂类分析标准品>>2053 N-己酰基 - 生物素 - 单唾液酸神经节苷脂GM1 N-Hexanoyl-biotin-monosialoganglioside GM1
Cat. Number
2053
Chemical Name
2053 N-己酰基 - 生物素 - 单唾液酸神经节苷脂GM1 N-Hexanoyl-biotin-monosialoganglioside GM1
Mol. Formula
C71H122N6O33S
Mol. Weight
1620
Qty 1
500µg
Appearance
solid
Application Notes
98+%,TLC; identity confirmed by MS
Synonym
Biotin-C6:0-GM1
Solubility
chloroform/methanol/water, 2:1:0.1
Storage condition
-20℃
References

Application Notes:

This ganglioside GM1 analogue contains a biotin unit attached to the amine of the sphingosine moiety via a hexanoic acid linker and is ideal for use in ganglioside studies. The biotin structure allows for attachment of the ganglioside to streptavidin and avidin substrates making it extremely useful for binding to substrates and for toxin detection.1 Gangliosides are acidic glycosphingolipids containing one or more sialic acids that generally form lipid rafts in the outer leaflet of the cell plasma membrane, especially in neuronal cells in the central nervous system.2,3 They participate in many cellular activities including proliferation, differentiation, adhesion, signal transduction, cell-to-cell interactions, tumorigenesis, and metastasis.4 The accumulation of gangliosides has been linked to several diseases including Tay-Sachs and Sandhoff disease while an autoimmune response against gangliosides can lead to Guillain-Barre syndrome. Gangliosides act as receptors for various toxins and bacteria, accumulate in various tumors, and aid in many neuronal functions. They are therefore very important in therapeutic processes and have warranted much research. GM1 stimulates neuronal sprouting and enhances the action of nerve growth factor (NGF) by directly and tightly associating with Trk, the high-affinity tyrosine kinase-type receptor for NGF. GM1 has also been identified as the specific cell surface receptor for cholera toxin making it an important target for therapeutic interventions.5

References: 
1. A. Pukin et al. Chemoenzymatic synthesis of biotin-appended analogues of gangliosides GM2, GM1, GD1a and GalNAc-GD1a for solid-phase applications and improved ELISA tests. Org. Biomol. Chem., 9(16):5809-5815, 2011 
2. L. Svennerholm, et al. (eds.), Structure and Function of Gangliosides, New York, Plenum, 1980 
3. T. Kolter, R. Proia, K. Sandhoff, Combinatorial Ganglioside Biosynthesis. J. Biol. Chem., July Vol. 277, No. 29, pp. 25859-25862, 2002 
4. S. Birkle, G. Zeng, L. Gao, R. K. Yu, and J. Aubry. Role of tumor-associated gangliosides in cancer progression. Biochimie, 85, 455–463, 2003 
5. C. E. Miller, J. Majewski, R. Faller, S. Satija, and T. L. Kuhl, Cholera Toxin Assault on Lipid Monolayers Containing Ganglioside GM1. Biophysj., June Vol. 86(6), 3700–3708, 2004

在线咨询 联系方式 二维码

服务热线

021-60498804

扫一扫,关注我们