790528P
Avanti
18:1 DGS-NTA
1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (ammonium salt), powder
Synonym(s):
1,2-di-(9Z-octadecenoyl)-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (ammonium salt); DOGS NTA
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About This Item
Empirical Formula (Hill Notation):
C53H100N5O13
CAS Number:
Molecular Weight:
1015.39
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
Recommended Products
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 5 mg (790528P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 790528P
shipped in
dry ice
storage temp.
−20°C
General description
Application
18:1 DGS-NTA 1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (ammonium salt) has been used:
- for generation of amphiphile monolayer [1]
- in NTA-liposome preparation for procoagulant binding studies and to study its effect on factor FXII autoactivation[2]
- as a liposome component for lipid bilayer preparation for surface plasmon resonance studies[3]
Biochem/physiol Actions
Packaging
5 mL Clear Glass Sealed Ampule (790528P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class
11 - Combustible Solids
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N J Mutch et al.
Journal of thrombosis and haemostasis : JTH, 10(10), 2108-2115 (2012-08-22)
Upon contact with an appropriate surface, factor XII (FXII) undergoes autoactivation or cleavage by kallikrein. Zn(2+) is known to facilitate binding of FXII and the cofactor, high molecular weight kininogen (HK), to anionic surfaces. To investigate whether transition metal ions
Louis Gioia et al.
Science immunology, 4(38) (2019-09-01)
The class II region of the major histocompatibility complex (MHC) locus is the main contributor to the genetic susceptibility to type 1 diabetes (T1D). The loss of an aspartic acid at position 57 of diabetogenic HLA-DQβ chains supports this association;
Decorating liquid crystal surfaces with proteins for real-time detection of specific protein-protein binding
Hartono D, et al.
Advances in Functional Materials, 19(22), 3574-3579 (2009)
Ronald D Seidel et al.
Journal of the American Chemical Society, 129(15), 4834-4839 (2007-03-28)
The study of bound-state conformations of ligands interacting with proteins is important to the understanding of protein function and the design of drugs that alter function. Traditionally, transferred nuclear Overhauser effects (trNOEs), measured from NMR spectra of ligands in rapid
C Dietrich et al.
Biochemistry, 35(4), 1100-1105 (1996-01-30)
The coupling of a DNA-binding protein to self-organized lipid monolayers is examined at the air-water interface by means of film balance techniques and epifluorescence microscopy. We used two recombinant species of the heat shock factor HSF24 which differ only in
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