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重要文件

810603C

Avanti

16:0-10 Doxyl PC

Avanti Research - A Croda Brand 810603C

同義詞:

1-palmitoyl-2-stearoyl-(10-doxyl)-sn-glycero-3-phosphocholine

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About This Item

經驗公式(希爾表示法):
C46H90N2O10P
CAS號碼:
分子量::
862.19
MDL號碼:
分類程式碼代碼:
41141825
NACRES:
NA.12
暫時無法取得訂價和供貨情況

化驗

>99% (TLC)

形狀

liquid

包裝

pkg of 1 × 1 mL (810603C-1mg)

製造商/商標名

Avanti Research - A Croda Brand 810603C

濃度

1 mg/mL (810603C-1mg)

脂質類型

ESR probes
phospholipids

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

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.[1][2]
Phosphocholine is considered as a precursor molecule. It is formed during the breakdown of phosphatidylcholine metabolism.[3]

應用

16:0-10 Doxyl PC may be used in vesicles for quenching PT-(1–46)F4W fluorescence.[4] 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.[5]

生化/生理作用

Phosphatidylcholine (PC) lowers the levels of cholesterol and triglycerides.[6]

包裝

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

準備報告

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.[7] For liposome preparations in fluorescent quenching measurements, dissolve the doxyl lipid in 150 μl absolute ethanol for a concentration of 40.3 mM [2], Additional supplemental information.

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形圖

Skull and crossbonesHealth hazard

訊號詞

Danger

危險分類

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

標靶器官

Central nervous system, Liver,Kidney

水污染物質分類(WGK)

WGK 3


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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
Phosphatidylserine dynamics in cellular membranes.
Kay, J.G
Molecular Biology of the Cell, 23, 2198-2212 (2012)
Insight into antibody combining sites using nuclear magnetic resonance and spin label haptens
McConnell HM
Advances in Protein Chemistry, 49, 135-148 (1996)

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