所有图片(1)
别名:
N-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-D-glucosyl-β1-1′-sphingosine
经验公式（希尔记法）:
C36H59N5O11
推荐产品
检测方案
>99% (TLC)
形式
powder
包装
pkg of 1 × 1 mg (810222P-1MG)
pkg of 1 × 250 μg (810222P-250ug)
制造商/商品名称
Avanti Polar Lipids 810222P
运输
dry ice
储存温度
−20°C
生化/生理作用
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.
包装
5 mL Amber Glass Screw Cap Vial (810299P-1MG)
5 mL Clear Glass Sealed Ampule (810222P-250ug)
WGK
WGK 3
闪点(°F)
No data available
闪点(°C)
No data available
法规信息
新产品
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)
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