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810603C

Avanti

16:0-10 Doxyl PC

Avanti Polar Lipids 810603C

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别名:
1-palmitoyl-2-stearoyl-(10-doxyl)-sn-glycero-3-phosphocholine
Empirical Formula (Hill Notation):
C46H90N2O10P
分子量:
862.19

检测方案

>99% (TLC)

形式

liquid

包装

pkg of 1 × 1 mL (810603C-1mg)

manufacturer/tradename

Avanti Polar Lipids 810603C

浓度

1 mg/mL (810603C-1mg)

lipid type

ESR probes
phospholipids

运输

dry ice

储存温度

−20°C

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此商品
810603P810604P810604C
16:0-10 Doxyl PC Avanti Polar Lipids 810603C

Avanti

810603C

16:0-10 Doxyl PC

16:0-10 Doxyl PC Avanti Polar Lipids 810603P, powder

Avanti

810603P

16:0-10 Doxyl PC

16:0-16 Doxyl PC Avanti Polar Lipids 810604P, powder

Avanti

810604P

16:0-16 Doxyl PC

16:0-16 Doxyl PC Avanti Polar Lipids 810604C

Avanti

810604C

16:0-16 Doxyl PC

form

liquid

form

powder

form

powder

form

liquid

packaging

pkg of 1 × 1 mL (810603C-1mg)

packaging

pkg of 1 × 1 mg (810603P-1mg)

packaging

pkg of 1 × 1 mg (810604P-1mg)

packaging

pkg of 1 × 1 mL (810604C-1mg)

concentration

1 mg/mL (810603C-1mg)

concentration

-

concentration

-

concentration

1 mg/mL (810604C-1mg)

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

manufacturer/tradename

Avanti Polar Lipids 810603C

manufacturer/tradename

Avanti Polar Lipids 810603P

manufacturer/tradename

Avanti Polar Lipids 810604P

manufacturer/tradename

Avanti Polar Lipids 810604C

一般描述

Avanti′s nitroxide spin product listing is a group of compounds designed to act as membrane probes. A variety of positions down the hydrophobic chain are labeled with the nitroxide functional groups to allow probing the membrane at various depths. These compounds have been synthesized from 1-palmitoyl-2-hydroxy-sn-glycerol-3-phosphocholine with the product being purified by column chromatography. Various n-doxyl phosphocholines have been recently used as biophysical tools to elucidate membrane trafficking with phosphatidylinositol transfer proteins and as fluorescent quenchers in lipid bilayer structural studies.
Phosphocholine is considered as a precursor molecule. It is formed during the breakdown of phosphatidylcholine metabolism.

应用

16:0-10 Doxyl PC may be used in vesicles for quenching PT-(1–46)F4W fluorescence. It may also be used in vesicles to check the fluorescence emission spectra in order to measure the penetration depth of the peptides′ tryptophan residues in lipid bilayer.

生化/生理作用

Phosphatidylcholine (PC) lowers the levels of cholesterol and triglycerides.

包装

5 mL Clear Glass Sealed Ampule (810603C-1mg)

制备说明

Product use: To prevent aggregation, prepare water-based solutions of 2 mM stock solutions of n-DOXYL PCs and store in plastic. Dilute stock solutions to 0.03- 0.1 mM solutions for EPR studies. For liposome preparations in fluorescent quenching measurements, dissolve the doxyl lipid in 150 μl absolute ethanol for a concentration of 40.3 mM , Additional supplemental information.

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

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

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Biology-cancer metabolic phenotype
NMR Metabolomics in Cancer Research, 15-138 (2013)
Q Wang et al.
Biochimica et biophysica acta, 1324(1), 69-75 (1997-02-21)
The N-terminal signal sequence of glucitol permease of Escherichia coli (Gut22: MIETITPGAVWFIGLFQKGGEC) and its analog (Gut22Ana: MIETITHGAEWFIGLFQKGGEC) were synthesized. The analog had a Pro residue substituted for the His at the 7th position of Gut22 and a Val residue substituted
L A Falls et al.
The Journal of biological chemistry, 276(26), 23895-23902 (2001-04-20)
The hydrophobic omega-loop within the prothrombin gamma-carboxyglutamic acid-rich (Gla) domain is important in membrane binding. The role of this region in membrane binding was investigated using a synthetic peptide, PT-(1-46)F4W, which includes the N-terminal 46 residues of human prothrombin with
Insight into antibody combining sites using nuclear magnetic resonance and spin label haptens
McConnell HM
Advances in Protein Chemistry, 49, 135-148 (1996)
Ultra-stable temperature control in EPR experiments: thermodynamics of gel-to-liquid phase transition in spin-labeled phospholipid bilayers and bilayer perturbations by spin labels
Alaouie AM, et. al.
Journal of Magnetic Resonance, 182, 229-238 (2006)

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