810222P
Avanti
C6-NBD Glucosyl Ceramide
Avanti Research™ - A Croda Brand 810222P, powder
Synonym(s):
N-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-D-glucosyl-β1-1′-sphingosine
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About This Item
Empirical Formula (Hill Notation):
C36H59N5O11
CAS Number:
Molecular Weight:
737.88
UNSPSC Code:
12352211
NACRES:
NA.25
Recommended Products
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
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
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
No data available
flash_point_c
No data available
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
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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