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方案
>99% (TLC)
表单
powder
包装
pkg of 1 × 1 mg (810156P-1mg)
制造商/商品名称
Avanti Research™ - A Croda Brand 810156P
运输
dry ice
储存温度
−20°C
一般描述
N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) phosphoethanolamine (NBD PE) is a fluorescently labeled lipid where NBD is attached to the headgroup of phosphatidylethanolamine (PE). PE is an aminophospholipid abundant in brain.
应用
18:1-06:0 NBD PE or 1-oleoyl-2-{12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl}-sn-glycero-3-phosphoethanolamine may be used as a component of liposome in cross-linking experiment and to determine M13 protein coat towards phospholipids.
生化/生理作用
N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) phosphoethanolamine (NBD PE) plays a key role as a fluorescent analog in the studies of organization and dynamics of membranes. NBD PE contributes to monitoring Red edge excitation shift (REES) effects, with the unique motional and dielectric properties it possesses.
包装
5 mL Amber Glass Screw Cap Vial (810156P-1mg)
法律信息
Avanti Research is a trademark of Avanti Polar Lipids, LLC
储存分类代码
11 - Combustible Solids
Fábio Fernandes et al.
Biophysical journal, 87(1), 344-352 (2004-07-09)
Quantification of lipid selectivity by membrane proteins has been previously addressed mainly from electron spin resonance studies. We present here a new methodology for quantification of protein-lipid selectivity based on fluorescence resonance energy transfer. A mutant of M13 major coat
Cardiolipin and phosphatidylethanolamine role in dibucaine interaction with the mitochondrial membrane
Lopes SC, et al.
Biochimica et Biophysica Acta - Biomembranes, 1861(6), 1152-1161 (2019)
Fluorescent methods to study biological membranes, 37-50 (2012)
Quantification of Protein-Lipid Selectivity using FRET: Application to the M13 Major Coat Protein
Fabio F, et al.
Journal of biophysics (Hindawi Publishing Corporation : Online), 87(1), 344-352 (2004)
Eun A Ra et al.
Nature communications, 7, 11726-11726 (2016-05-25)
Autophagy is responsible for the bulk degradation of cytosolic constituents and plays an essential role in the intestinal epithelium by controlling beneficial host-bacterial relationships. Atg5 and Atg7 are thought to be critical for autophagy. However, Atg5- or Atg7-deficient cells still
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