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870285P

Avanti

16:0 Biotinyl PE

Avanti Research™ - A Croda Brand 870285P, powder

Synonyme(s) :

1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl) (sodium salt)

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About This Item

Formule empirique (notation de Hill):
C47H87N3O10PNaS
Numéro CAS:
384835-54-5
Poids moléculaire :
940.24
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Forme

powder

Conditionnement

pkg of 1 × 100 mg (870285P-100mg)
pkg of 1 × 200 mg (870285P-200mg)
pkg of 1 × 25 mg (870285P-25mg)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand 870285P

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(OCCN([H])C(CCCC[C@](SC[C@@]1(NC(N2)=O)[H])([C@]12[H])[H])=O)=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C47H88N3O10PS.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-33-44(52)57-37-40(60-45(53)34-28-26-24-22-20-18-16-14-12-10-8-6-4-2)38-59-61(55,56)58-36-35-48-43(51)32-30-29-31-42-46-41(39-62-42)49-47(54)50-46;/h40-42,46H,3-39H2,1-2H3,(H,48,51)(H,55,56)(H2,49,50,54);/q;+1/p-1/t40-,41+,42+,46+;/m1./s1

Clé InChI

ZBLHTNMJPDLJFU-DISIHPEUSA-M

Description générale

16:0 Biotinyl PE, also referred as 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl) (biotin-DPPE), belongs to a class of head group modified functionalized lipids. Functionalized lipids act as reporter molecules.

Application

18:1 Biotinyl PE has been used: as a standard component in preparation of mixed micelles, in preparation of phase-separated giant unilamellar vesicles (GUVs), as a component of lipid mixture for fluorescence imaging labeling, in the preparation of lipid bilayers.

Conditionnement

5 mL Amber Glass Screw Cap Vial (870285P-100mg)
5 mL Amber Glass Screw Cap Vial (870285P-200mg)
5 mL Amber Glass Screw Cap Vial (870285P-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids

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Taeho Ahn et al.
Protein expression and purification, 101, 37-41 (2014-06-04)
Recombinant cytochrome P450 (CYP or P450) enzymes are useful for drug metabolism research and thereby many expression and purification systems have been developed. Here, we provide a method for the purification of human P450s 3A4 and 1A2 expressed in Escherichia
Hyun-Sook Jang et al.
Biomaterials science, 7(4), 1393-1398 (2019-01-22)
We demonstrate a method to prepare giant unilamellar vesicles (GUVs) with biologically-active protein activity, by mixing erythrocyte (red blood cell) membrane extract with phospholipids and growing their mixture in a porous hydrogel matrix. This presents a pathway to retain protein
Cornelia A Hermann et al.
Analytical and bioanalytical chemistry (2020-02-20)
Magnetized liposome (magnetosomes) labels can overcome diffusion limitations in bioassays through fast and easy magnetic attraction. Our aim therefore was to advance the understanding of factors influencing their synthesis focusing on encapsulation strategies and synthesis parameters. Magnetosome synthesis is governed
Daniel L Burden et al.
Langmuir : the ACS journal of surfaces and colloids, 34(37), 10847-10855 (2018-08-29)
All cells in all domains of life possess a cytoskeleton that provides mechanical resistance to deformation and general stability to the plasma membrane. Here, we utilize a two-dimensional scaffolding created by actin filaments to convey mechanical support upon relatively fragile
Carola Hofmann et al.
Analytical and bioanalytical chemistry, 412(14), 3383-3393 (2020-04-07)
Liposomes have been widely applied in bioanalytical assays. Most liposomes used bare negative charges to prevent non-specific binding and increase colloidal stability. Here, in contrast, highly stable, positively charged liposomes entrapping the fluorescent dye sulforhodamine B (SRB) were developed to
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