추천 제품
형태
liquid
포장
pkg of 1 × 10 mg (861809O-10mg)
pkg of 1 × 100 mg (861809O-100mg)
제조업체/상표
Avanti Research™ - A Croda Brand
배송 상태
dry ice
저장 온도
−20°C
일반 설명
Oleic acid-d9 is a deuterated derivative of oleic acid. Oleic acid is important for structure and function of cellular membranes. It is widely used in nuclear magnetic resonance, infrared, mass spectroscopy and neutron scattering studies.
애플리케이션
Oleic acid-d9 has been used for spiking Alexidine treatment media during preparation of sample for liquid chromatography-mass spectrometry (LC-MS) analysis.
포장
5 mL Clear Glass Sealed Ampule (861809O-100mg)
5 mL Clear Glass Sealed Ampule (861809O-10mg)
법적 정보
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
10 - Combustible liquids
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
High-content screen for modifiers of Niemann-Pick type C disease in patient cells
Pugach EK, et al.
Human Molecular Genetics, 27(12), 2101-2112 (2018)
Synthesis of deuterated [D32] oleic acid and its phospholipid derivative [D64] dioleoyl-sn-glycero-3-phosphocholine
Darwish TA, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 56(9-10), 520-529 (2013)
Tamim A Darwish et al.
Journal of labelled compounds & radiopharmaceuticals, 56(9-10), 520-529 (2013-11-29)
Oleic acid and its phospholipid derivatives are fundamental to the structure and function of cellular membranes. As a result, there has been increasing interest in the availability of their deuterated forms for many nuclear magnetic resonance, infrared, mass spectroscopy and
Siddabasave Gowda B Gowda et al.
Rapid communications in mass spectrometry : RCM, 34(17), e8831-e8831 (2020-05-18)
Fatty acid esters of hydroxy fatty acids (FAHFAs) are recently discovered endogenous lipids with outstanding health benefits. FAHFAs are known to exhibit antioxidant, antidiabetic and anti-inflammatory properties. The number of known long-chain FAHFAs in mammalian tissues and dietary resources increased
Emily K Pugach et al.
Human molecular genetics, 27(12), 2101-2112 (2018-04-17)
Niemann-Pick type C (NPC) disease is a rare lysosomal storage disease caused primarily by mutations in NPC1. NPC1 encodes the lysosomal cholesterol transport protein NPC1. The most common NPC1 mutation is a missense mutation (NPC1I1061T) that causes misfolding and rapid
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