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Merck
CN

999988P

Avanti

13:0 Diether PC

Avanti Research - A Croda Brand

别名:

1,2-di-O-tridecyl-sn-glycero-3-phosphocholine

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关于此项目

经验公式(希尔记法):
C34H72NO6P
化学文摘社编号:
分子量:
621.91
MDL number:
UNSPSC Code:
51191904
NACRES:
NA.25
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产品名称

13:0 Diether PC, Avanti Research - A Croda Brand 999988P, powder

InChI

1S/C34H72NO6P/c1-6-8-10-12-14-16-18-20-22-24-26-29-38-32-34(33-41-42(36,37)40-31-28-35(3,4)5)39-30-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1

InChI key

BEBKMIWGRRQYKZ-UUWRZZSWSA-N

SMILES string

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OCCCCCCCCCCCCC)COCCCCCCCCCCCCC)=O

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 10 mg (999988P-10mg)

manufacturer/tradename

Avanti Research - A Croda Brand 999988P

lipid type

phospholipids
cardiolipins

shipped in

dry ice

storage temp.

−20°C

Packaging

5 mL Amber Glass Screw Cap Vial (999988P-10mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Application

13:0 Diether PC or 1,2-di-O-tridecyl-sn-glycero-3-phosphocholine is suitable for bicelle preparation and as an internal standard for lipid identification in tissue.

Biochem/physiol Actions

13:0 Diether PC (phosphocholine) is useful for bicelles preparation. Bicelles can be integrated into standard crystallization protocols and in contrast to micelles, bicelles maintain the protein in a more native bilayer environment allowing proteins to be captured in a more biologically relevant orientation.

General description

13:0 Diether PC (phosphocholine) is a class of glycerophospholipids that has two tridecane chains attached to the sn-1 and sn-2 positions of the glycerol backbone by ether bonds. It has choline as the alcohol moiety, attached to the phosphate group.

存储类别

11 - Combustible Solids

wgk

WGK 3

法规信息

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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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Christian Baumeier et al.
Biochimica et biophysica acta, 1851(5), 566-576 (2015-02-04)
Caloric restriction and intermittent fasting are known to improve glucose homeostasis and insulin resistance in several species including humans. The aim of this study was to unravel potential mechanisms by which these interventions improve insulin sensitivity and protect from type
Hugo F Azurmendi et al.
Carbohydrate research, 337(10), 905-915 (2002-05-15)
The conformations of two synthetic trisaccharides of blood group A and B (alpha-L-Fucp-(1-->2)-[alpha-D-GalpNAc-(1-->3)]-alpha-D-Galp and alpha-L-Fucp-(1-->2)-[alpha-D-Galp-(1-->3)]-alpha-D-Galp, respectively) and of a type A tetrasaccharide alditol, Fucp-(1-->2)-[alpha-D-GalpNAc-(1-->3)]-beta-D-Galp-(1-->3)-GalNAc-ol, were studied by NMR measurements of one-bond C-H residual dipolar couplings in partially oriented liquid crystal
John M Dean et al.
Protein & cell, 9(2), 196-206 (2017-05-20)
Ether lipids, such as plasmalogens, are peroxisome-derived glycerophospholipids in which the hydrocarbon chain at the sn-1 position of the glycerol backbone is attached by an ether bond, as opposed to an ester bond in the more common diacyl phospholipids. This

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