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Merck
CN

855779C

Avanti

22:0 Lyso PC

1-behenoyl-2-hydroxy-sn-glycero-3-phosphocholine, chloroform

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别名:
1-docosanoyl-sn-glycero-3-phosphocholine; PC(22:0/0:0)
经验公式(希尔记法):
C30H62NO7P
分子量:
579.79
UNSPSC代码:
51191904
NACRES:
NA.25

检测方案

>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)

形式

liquid

包装

pkg of 1 × 2.5 mL (855779C-25mg)

制造商/商品名称

Avanti Polar Lipids 855779C

浓度

10 mg/mL (855779C-25mg)

运输

dry ice

储存温度

−20°C

应用

22:0 Lyso PC has been used as a standard for liquid chromatography with tandem mass spectrometry (LC-MS/MS) analysis.

包装

5 mL Clear Glass Sealed Ampule (855779C-25mg)

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

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

靶器官

Central nervous system, Liver,Kidney

WGK

WGK 3

法规信息

易制毒化学品(2类)
危险化学品

分析证书(COA)

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The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders
Law KB, et al.
Autophagy, 13(5), 868-884 (2017)
Comprehensive untargeted lipidomic analysis using core-shell C30 particle column and high field orbitrap mass spectrometer
Narvaez-Rivas M and Zhang Q
Journal of Chromatography A, 1440, 123-134 (2016)
Francesca Saitta et al.
Colloids and surfaces. B, Biointerfaces, 186, 110715-110715 (2019-12-17)
A fifteen-components model membrane that reflected the 80 % of phospholipids present in Insulin Secretory Granules was obtained and thermodynamic exploitation was performed, through micro-DSC, in order to assess the synergic contributions to the stability of a mixed complex system
Kelsey B Law et al.
Autophagy, 13(5), 868-884 (2017-05-20)
Peroxisome biogenesis disorders (PBDs) are metabolic disorders caused by the loss of peroxisomes. The majority of PBDs result from mutation in one of 3 genes that encode for the peroxisomal AAA ATPase complex (AAA-complex) required for cycling PEX5 for peroxisomal
Mónica Narváez-Rivas et al.
Journal of chromatography. A, 1440, 123-134 (2016-03-02)
The goal of untargeted lipidomics is to have high throughput, yet comprehensive and unambiguous identification and quantification of lipids. Novel stationary phases in LC separation and new mass spectrometric instruments capable of high mass resolving power and faster scanning rate

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