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Merck
모든 사진(1)

주요 문서

790528P

Avanti

18:1 DGS-NTA

1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (ammonium salt), powder

동의어(들):

1,2-di-(9Z-octadecenoyl)-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (ammonium salt); DOGS NTA

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크기 선택

5 MG
₩235,480

₩235,480

출고 가능일2025년 4월 15일세부사항

벌크 견적 요청
모든 사진(1)

크기 선택

보기 변경
5 MG
₩235,480

About This Item

실험식(Hill 표기법):
C53H100N5O13
CAS Number:
474942-78-4
Molecular Weight:
1015.39
MDL number:
MFCD00057815
UNSPSC 코드:
12352211
NACRES:
NA.25

₩235,480

출고 가능일2025년 4월 15일세부사항

벌크 견적 요청

분석

>99% (TLC)

양식

powder

포장

pkg of 1 × 5 mg (790528P-5mg)

제조업체/상표

Avanti Research™ - A Croda Brand 790528P

배송 상태

dry ice

저장 온도

−20°C

일반 설명

1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (18:1 DGS-NTA) is amphiphile.[1] DGS-NTA is a nitrilotriacetic acid -functionalized amphiphile devoid of nickel ion.[1]

애플리케이션

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]

생화학적/생리학적 작용

1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl)iminodiacetic acid)succinyl] (18:1 DGS-NTA or DOGS-NTA) cannot bind to histidine due to lack of nickel ion. It is capable of self-assembly to form a stable monolayer.[1] DOGS-NTA ammonium salt is useful in bicelle preparation. [4]

포장

5 mL Clear Glass Sealed Ampule (790528P-5mg)

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

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
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;
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
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)
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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