跳轉至內容
Merck
全部照片(1)

重要文件

810222P

Avanti

C6-NBD Glucosyl Ceramide

Avanti Research - A Croda Brand 810222P, powder

同義詞:

N-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-D-glucosyl-β1-1′-sphingosine

登入查看組織和合約定價


About This Item

經驗公式(希爾表示法):
C36H59N5O11
CAS號碼:
分子量::
737.88
MDL號碼:
分類程式碼代碼:
12352211
NACRES:
NA.25

化驗

>99% (TLC)

形狀

powder

包裝

pkg of 1 × 1 mg (810222P-1MG)
pkg of 1 × 250 μg (810222P-250ug)

製造商/商標名

Avanti Research - A Croda Brand 810222P

運輸包裝

dry ice

儲存溫度

−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.

包裝

5 mL Amber Glass Screw Cap Vial (810299P-1MG)
5 mL Clear Glass Sealed Ampule (810222P-250ug)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如果您需要協助,請聯絡 客戶支援

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

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)

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務