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Merck
CN

810227C

Avanti

C12-NBD Lactosyl Ceramide

Avanti Research - A Croda Brand

别名:

N-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-D-lactosyl-β1-1′-sphingosine

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关于此项目

经验公式(希尔记法):
C48H81N5O16
化学文摘社编号:
分子量:
984.18
UNSPSC代码:
12352211
NACRES:
NA.25
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产品名称

C12-NBD Lactosyl Ceramide, Avanti Research - A Croda Brand 810227C

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 1 mL (810227C-50ug)

制造商/商品名称

Avanti Research - A Croda Brand 810227C

浓度

0.05 mg/mL (810227C-50ug)

运输

dry ice

储存温度

−20°C

一般描述

C12-NBD Lactosyl ceramide is a fluorescent derivative of the naturally occurring compound lactosyl ceramide, which is present on neutrophils and macrophages.

生化/生理作用

Lactosyl ceramide plays a key role in signaling cascades leading to phenotypic changes such as adhesion, migration, cell proliferation, and angiogenesis. In vertebrates, lactosyl ceramide is a major precursor for biosynthesis of glycosphingolipids involved in various vital cellular processes. Lactosyl ceramide is also known to be crucial for mediating osteoclastogenesis.

包装

5 mL Amber Glass Screw Cap Vial (810227C-50ug)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

靶器官

Central nervous system

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

闪点(°F)

does not flash

闪点(°C)

does not flash

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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T Iwamoto et al.
The Journal of biological chemistry, 276(49), 46031-46038 (2001-10-11)
Glycosphingolipids and their metabolites play important roles in a variety of biological processes. Several signal molecules are localized in a glycolipid-enriched microdomain on the cell surface, and their signals are regulated by the glycolipid composition. However, the function of glycolipids
S Hakomori et al.
Journal of biochemistry, 118(6), 1091-1103 (1995-12-01)
Glycosphingolipids (GSLs), cell type-specific markers which change dramatically during ontogenesis and oncogenesis, have been implicated as playing major roles in cellular interactions and control of cell proliferation in multicellular organisms. These functional roles have been partially clarified through two types
W I Weis et al.
Annual review of biochemistry, 65, 441-473 (1996-01-01)
Lectins are responsible for cell surface sugar recognition in bacteria, animals, and plants. Examples include bacterial toxins; animal receptors that mediate cell-cell interactions, uptake of glycoconjugates, and pathogen neutralization; and plant toxins and mitogens. The structural basis for selective sugar
Subroto Chatterjee et al.
Biochimica et biophysica acta, 1780(3), 370-382 (2007-12-14)
Although lactosylceramide (LacCer) plays a pivotal role in the biosynthesis of nearly all the major glycosphingolipids, its function in regulating cellular function has begun to emerge only recently. Our current opinion is that several physiologically critical molecules such as modified/oxidized
F Pincet et al.
Biophysical journal, 80(3), 1354-1358 (2001-02-27)
Carbohydrate-carbohydrate interactions are rarely considered in biologically relevant situations such as cell recognition and adhesion. One Ca(2+)-mediated homotypic interaction between two Lewis(x) determinants (Le(x)) has been proposed to drive cell adhesion in murine embryogenesis. Here, we confirm the existence of

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