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Merck
CN

810705P

Avanti

16-NBD-16:0辅酶A

Avanti Research - A Croda Brand 810705P, powder

别名:

25-[N-[(7-硝基-2-1,3-苯并恶二唑-4-基)甲基]氨基]-27-降胆甾醇{N-[(7-小计-2-1,3-苯并恶二唑-4-基)-甲基]氨基}棕榈酰基辅酶 A (铵盐)

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About This Item

经验公式(希尔记法):
C43H77N14O20P3S
分子量:
1235.14
UNSPSC代码:
12352211
NACRES:
NA.25

检测方案

>99% (TLC)

形式

powder

包装

pkg of 1 × 1 mg (810705P-1mg)

制造商/商品名称

Avanti Research - A Croda Brand 810705P

应用

lipidomics

脂质类型

coenzymes

运输

dry ice

储存温度

−20°C

SMILES字符串

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCCCCNC1=CC=C([N+]([O-])=O)C2=NON=C12)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]3OP([O-])(O)=O)O[C@H]([C@@H]3O)N4C5=C(C(N)=NC=N5)N=C4)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

一般描述

NBD-棕榈酰-CoA((N-[((7-硝基-2-1,3-苯并恶二唑-4-基)-甲基]氨基)棕榈酰辅酶A)是棕榈酰-CoA的荧光类似物。
产品可用于荧光标记蛋白质上的棕榈酰化位点。

应用

16-NBD-16:0辅酶A((N-[(7-硝基-2-1,3-苯并恶二唑-4-基)-甲基]氨基)棕榈酰辅酶A)已用于:
  • 作为荧光二酰基甘油酰基转移酶(DGAT)测定中的荧光底物
  • 作为荧光类似物,用于研究脂质的膜易位并跟踪棕榈酰-CoA的摄取
  • 作为洗涤缓冲液中的组分,用于测量棕榈酸酯转移酶测定中酶的自酰化

生化/生理作用

NBD-棕榈酰-CoA((N-[((7-硝基-2-1,3-苯并恶二唑-4-基)-甲基]氨基)棕榈酰辅酶A)可作为放射性示踪剂的经济替代品。

包装

5 mL琥珀色玻璃螺旋盖小瓶(810705P-1mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids


分析证书(COA)

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Xiaochao Wei et al.
Cell host & microbe, 11(2), 140-152 (2012-02-22)
The intestinal mucus barrier prevents pathogen invasion and maintains host-microbiota homeostasis. We show that fatty acid synthase (FAS), an insulin-responsive enzyme essential for de novo lipogenesis, helps maintain the mucus barrier by regulating Mucin 2, the dominant mucin in the
Maurine E Linder et al.
Biochemistry, 42(15), 4311-4320 (2003-04-16)
Since its discovery more than 30 years ago, protein palmitoylation has been shown to have a role in protein-membrane interactions, protein trafficking, and enzyme activity. Until recently, however, the molecular machinery that carries out reversible palmitoylation of proteins has been
S J Moench et al.
Biochemistry, 33(19), 5783-5790 (1994-05-17)
Two tandem cysteine residues in the carboxyl-terminal region of rhodopsin have been shown to be covalently linked to palmitate via thioester bonds (Ovchinnikov, Y. A., et al. (1988) FEBS Lett. 230, 1-5). We have synthesized a fluorescent analogue of palmitoyl
Pamela J McFie et al.
Journal of lipid research, 52(9), 1760-1764 (2011-06-10)
Triacylglycerols (TG) are the major storage form of energy in eukaryotic organisms and are synthesized primarily by acyl CoA:1,2-diacylglycerol acyltransferase (DGAT) enzymes. In vitro DGAT activity has previously been quantified by measuring the incorporation of either radiolabeled fatty acyl CoA
Raffaello Verardi et al.
Structure (London, England : 1993), 25(9), 1337-1347 (2017-08-02)
DHHC enzymes catalyze palmitoylation, a major post-translational modification that regulates a number of key cellular processes. There are up to 24 DHHCs in mammals and hundreds of substrate proteins that get palmitoylated. However, how DHHC enzymes engage with their substrates

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