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Merck
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870277P

Avanti

16:0 Biotinyl Cap PE

Avanti Research™ - A Croda Brand

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C53H98N4O11PNaS
CAS Number:
384835-52-3
Molecular Weight:
1053.39
MDL number:
MFCD22495347
UNSPSC Code:
12352211
NACRES:
NA.25

Key Documents

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Product Name

16:0 Biotinyl Cap PE, Avanti Research™ - A Croda Brand 870277P, powder

SMILES string

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

InChI

1S/C53H99N4O11PS.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-29-37-50(60)65-42-45(68-51(61)38-30-26-24-22-20-18-16-14-12-10-8-6-4-2)43-67-69(63,64)66-41-40-55-49(59)35-28-27-33-39-54-48(58)36-32-31-34-47-52-46(44-70-47)56-53(62)57-52;/h45-47,52H,3-44H2,1-2H3,(H,54,58)(H,55,59)(H,63,64)(H2,56,57,62);/q;+1/p-1/t45-,46+,47+,52+;/m1./s1

InChI key

HLOYGXYDOICSBP-OHXMQTJZSA-M

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 100 mg (870277P-100mg)
pkg of 1 × 25 mg (870277P-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870277P

shipped in

dry ice

storage temp.

−20°C

Application

16:0 Biotinyl Cap PE has been used in preparation of lipid vesicles. It has also been used in nanodisc preparation.

General description

16:0 Biotinyl Cap PE, also known as 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(cap biotinyl) is a head group modified lipid containing biotinyl cap PE.

Packaging

5 mL Amber Glass Screw Cap Vial (870277P-100mg)
5 mL Amber Glass Screw Cap Vial (870277P-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

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Charlotte Larsson et al.
Analytical chemistry, 75(19), 5080-5087 (2004-01-08)
We show how the water content (and effective density) of thin adsorbed films composed of biomolecules can be determined using combined quartz crystal microbalance with dissipation monitoring (QCM-D) and surface plasmon resonance (SPR) analysis. In particular, these techniques, combined with
Bianca Buchegger et al.
Analytical chemistry, 90(21), 12372-12376 (2018-10-24)
Mobility of proteins and lipids plays a major role in physiological processes. Platforms which were developed to study protein interaction between immobilized and mobile proteins suffer from shortcomings such as fluorescence quenching or complicated fabrication methods. Here we report a
Rajan Lamichhane et al.
Bio-protocol, 7(12) (2017-11-25)
Activation of G protein-coupled receptors (GPCRs) by agonist ligands is mediated by a transition from an inactive to active receptor conformation. We describe a novel single-molecule assay that monitors activation-linked conformational transitions in individual GPCR molecules in real-time. The receptor
Carol Cho et al.
Nature communications, 10(1), 5764-5764 (2019-12-19)
The fundamental unit of chromatin, the nucleosome, is an intricate structure that requires histone chaperones for assembly. ATAD2 AAA+ ATPases are a family of histone chaperones that regulate nucleosome density and chromatin dynamics. Here, we demonstrate that the fission yeast ATAD2
David Garenne et al.
Biomacromolecules, 21(7), 2808-2817 (2020-05-23)
Building genetically programmed synthetic cell systems by molecular integration is a powerful and effective approach to capture the synergies between biomolecules when they are put together. In this work, we characterized quantitatively the effects of molecular crowding on gene expression
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