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870285P

Avanti

16:0 Biotinyl PE

Avanti Research - A Croda Brand 870285P, powder

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C47H87N3O10PNaS
CAS Number:
Molecular Weight:
940.24
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

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

manufacturer/tradename

Avanti Research - A Croda Brand 870285P

shipped in

dry ice

storage temp.

−20°C

SMILES string

[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

InChI key

ZBLHTNMJPDLJFU-DISIHPEUSA-M

General description

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.

Packaging

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)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Zachary I Imam et al.
Langmuir : the ACS journal of surfaces and colloids, 35(49), 16281-16289 (2019-11-16)
Cytoskeletal filaments and motor proteins are critical components in the transport and reorganization of membrane-based organelles in eukaryotic cells. Previous studies have recapitulated the microtubule-kinesin transport system in vitro to dynamically assemble large-scale nanotube networks from multilamellar liposomes and polymersomes.
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
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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