登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C36H59N5O11
化学文摘社编号:
分子量:
737.88
MDL number:
NACRES:
NA.25
UNSPSC Code:
12352211
产品名称
C6-NBD Glucosyl Ceramide, Avanti Research™ - A Croda Brand 810222P, powder
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (810222P-1MG), pkg of 1 × 250 μg (810222P-250ug)
manufacturer/tradename
Avanti Research™ - A Croda Brand 810222P
shipped in
dry ice
storage temp.
−20°C
正在寻找类似产品? 访问 产品对比指南
Biochem/physiol Actions
The synthesis of glucosyl ceramide (GlcCer) occurs in the cytosolic membranes of Golgi. It is catalysed by GlcCer synthase. In the luminal Golgi membrane, GlcCer participates in the generation of glycosphingolipids. C6-NBD glcCer is useful to view ceramide rich membrane domains in Golgi compartments.
Packaging
5 mL Amber Glass Screw Cap Vial (810299P-1MG)
5 mL Clear Glass Sealed Ampule (810222P-250ug)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
No data available
flash_point_c
No data available
法规信息
新产品
此项目有
A functionalized sphingolipid analogue for studying redistribution during activation in living T cells
Collenburg L, et al.
Journal of Immunology, 196(9), 3951-3962 (2016)
Glycosphingolipid synthesis requires FAPP2 transfer of glucosylceramide
D?Angelo G, et al.
Nature, 449(7158), 62-62 (2007)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持