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Principaux documents

870282C

Avanti

18:1 Biotinyl PE

Avanti Research - A Croda Brand 870282C

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C51H91N3O10PNaS
Numéro CAS:
Poids moléculaire :
992.31
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Forme

liquid

Conditionnement

pkg of 1 × 2.5 mL (870282C-25mg)
pkg of 1 × 4 mL (870282C-100mg)
pkg of 2 × 4 mL (870282C-200mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand 870282C

Concentration

10 mg/mL (870282C-25mg)
25 mg/mL (870282C-100mg)
25 mg/mL (870282C-200mg)

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(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O.[Na+]

InChI

1S/C51H92N3O10PS.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-37-48(56)61-41-44(64-49(57)38-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)42-63-65(59,60)62-40-39-52-47(55)36-34-33-35-46-50-45(43-66-46)53-51(58)54-50;/h17-20,44-46,50H,3-16,21-43H2,1-2H3,(H,52,55)(H,59,60)(H2,53,54,58);/q;+1/p-1/b19-17-,20-18-;/t44-,45+,46+,50+;/m1./s1

Clé InChI

ZGFSYDGJPSEMJM-AOAFAMOJSA-M

Description générale

18:1 Biotinyl PE, also referred as 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl), belongs to a class of head group modified functionalized lipids.

Application

18:1 Biotinyl PE is suitable: to tag N-glycolyl-monosialodihexosyl-ganglioside (NGcGM3) in the competitive assay, in preparation of small unilamellar vesicle, to test the functionalization of Polydimethylsiloxane (PDMS) polymer.

Conditionnement

5 mL Clear Glass Sealed Ampule (870282C-100mg)
5 mL Clear Glass Sealed Ampule (870282C-200mg)
5 mL Clear Glass Sealed Ampule (870282C-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system, Liver,Kidney

Code de la classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


Certificats d'analyse (COA)

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Les clients ont également consulté

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1 of 1

H Zhan
Journal of biochemical and biophysical methods, 41(1), 13-19 (1999-10-08)
A general method for measuring interaction of liposome-protein (or potentially small molecules) was developed. This method utilizes biotinylated liposomes to incubate with interactants. Streptavidin-coated paramagnetic resins were then added and the liposomes (along with bound materials) can be quickly separated
Bo Huang et al.
Lab on a chip, 6(3), 369-373 (2006-03-03)
Polydimethylsiloxane (PDMS) surfaces can be functionalized with biotin groups by adding biotinylated phospholipids to the PDMS prepolymer before curing. The addition of beta-D-dodecyl-N-maltoside (DDM) in the solution blocks non-specific protein binding on these functionalized PDMS surfaces. We characterize the surface
M Virginia Gentilini et al.
Cancer immunology, immunotherapy : CII, 65(5), 551-562 (2016-03-13)
The expression of N-glycolyl-monosialodihexosyl-ganglioside (NGcGM3) in humans is restricted to cancer cells; therefore, it is a tumor antigen. There are measurable quantities of circulating anti-NGcGM3 antibodies (aNGcGM3 Abs) in human serum. Interestingly, some people have circulating Ag-specific immunoglobulins G (IgGs)
Ingrid Albertsson et al.
Scientific reports, 9(1), 17234-17234 (2019-11-23)
Denitrification is a microbial pathway that constitutes an important part of the nitrogen cycle on earth. Denitrifying organisms use nitrate as a terminal electron acceptor and reduce it stepwise to nitrogen gas, a process that produces the toxic nitric oxide
Heun Jin Lee et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(49), 19253-19257 (2008-12-03)
Recent advances have enabled 3-dimensional reconstructions of biological structures in vivo, ranging in size and complexity from single proteins to multicellular structures. In particular, tomography and confocal microscopy have been exploited to capture detailed 3-dimensional conformations of membranes in cellular

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

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