检测方案
>99% (TLC)
形式
liquid
包装
pkg of 1 × 1 mL (810150C-1mg)
pkg of 5 × 1 mL (810150C-5mg)
pkg of 5 × 2 mL (810150C-10mg)
制造商/商品名称
Avanti Research™ - A Croda Brand
浓度
1 mg/mL (810150C-10mg)
1 mg/mL (810150C-1mg)
1 mg/mL (810150C-5mg)
运输
dry ice
储存温度
−20°C
一般描述
L-α-磷脂酰乙醇胺（PE）是动植物和酵母中含量第二高的磷脂。
应用
18：1 Liss Rhod PE适用于标记DOPC（1,2-油酰基-sn-甘油-3-磷酸胆碱）以进行成像。
生化/生理作用
18：1 Liss Rhod PE是一种荧光标记的脂质，可用于标记巨型单层囊泡（giant unilamellar vesicle，GUV）。L-α-磷脂酰乙醇胺可保持膜完整性。
包装
5 mL棕色玻璃螺旋盖小瓶（810150C-10mg）
5 mL棕色玻璃螺旋盖小瓶（810150C-1mg）
5 mL棕色玻璃螺旋盖小瓶（810150C-5mg）
法律信息
Avanti Research is a trademark of Avanti Polar Lipids, LLC
通常也和此产品一起购买
产品编号
说明
价格
警示用语：
Danger
危险分类
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
靶器官
Central nervous system, Liver,Kidney
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
危险化学品
易制毒化学品（2类）
Spatiotemporal control of coacervate formation within liposomes
Deshpande S, et al.
Nature Communications, 10(1), 1800-1800 (2019)
A new class of synthetic retinoid antibiotics effective against bacterial persisters
Kim W, et al.
Nature, 556(7699), 103-103 (2018)
Stabilization of liposomes against stress using polyelectrolytes: Interaction mechanisms, influence of pH, molecular weight, and polyelectrolyte structure
Rinaudo M, et al.
International Journal of Polymer Analysis and Characterization, 14(8), 667-677 (2009)
Yachong Guo et al.
ACS nano (2018-11-20)
Increasing awareness of bioeffects and toxicity of nanomaterials interacting with cells puts in focus the mechanisms by which nanomaterials can cross lipid membranes. Apart from well-discussed energy-dependent endocytosis for large objects and passive diffusion through membranes by solute molecules, other
Yang Liu et al.
Nature communications, 10(1), 5108-5108 (2019-11-11)
Mounting evidence suggests that the tumor microenvironment is profoundly immunosuppressive. Thus, mitigating tumor immunosuppression is crucial for inducing sustained antitumor immunity. Whereas previous studies involved intratumoral injection, we report here an inhalable nanoparticle-immunotherapy system targeting pulmonary antigen presenting cells (APCs)
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