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Merck

810150C

Avanti

18:1 Liss Rhod PE

Avanti Research - A Croda Brand

Sinônimo(s):

1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(lissamine rhodamine B sulfonyl) (ammonium salt)

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Sobre este item

Fórmula empírica (Notação de Hill):
C68H109N4O14PS2
Número CAS:
Peso molecular:
1301.72
MDL number:
NACRES:
NA.25
UNSPSC Code:
12352211

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assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 1 mL (810150C-1mg), pkg of 5 × 1 mL (810150C-5mg), pkg of 5 × 2 mL (810150C-10mg)

manufacturer/tradename

Avanti Research - A Croda Brand

concentration

1 mg/mL (810150C-10mg), 1 mg/mL (810150C-1mg), 1 mg/mL (810150C-5mg)

lipid type

fluorescent lipids

shipped in

dry ice

storage temp.

−20°C

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General description

L-α-Phosphatidylethanolamine (PE) is the second most abundant phospholipid in animals, plants and yeast.[1]

Application

18:1 Liss Rhod PE suitable to be used for labelling DOPC (1,2-dioleoyl-sn-glycero-3-phosphocholine) for visualization purpose.[2]

Biochem/physiol Actions

18:1 Liss Rhod PE is a fluorescent labelled lipid,[3] useful in labelling giant unilamellar vesicles (GUVs).[4] L-α-Phosphatidylethanolamine maintains maembrane integrity.[5]

Packaging

5 mL Amber Glass Screw Cap Vial (810150C-10mg)
5 mL Amber Glass Screw Cap Vial (810150C-1mg)
5 mL Amber Glass Screw Cap Vial (810150C-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system, Liver,Kidney

Classe de armazenamento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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A new class of synthetic retinoid antibiotics effective against bacterial persisters
Kim W, et al.
Nature, 556(7699), 103-103 (2018)
Spatiotemporal control of coacervate formation within liposomes
Deshpande S, et al.
Nature Communications, 10(1), 1800-1800 (2019)
Stabilization of liposomes against stress using polyelectrolytes: Interaction mechanisms, influence of pH, molecular weight, and polyelectrolyte structure
Rinaudo M, et al.
International Journal of Polymer Analysis and Characterization, 14(8), 667-677 (2009)
Yachong Guo et al.
ACS nano (2018-11-20)
Increasing awareness of bioeffects and toxicity of nanomaterials interacting with cells puts in focus the mechanisms by which nanomaterials can cross lipid membranes. Apart from well-discussed energy-dependent endocytosis for large objects and passive diffusion through membranes by solute molecules, other
Yang Liu et al.
Nature communications, 10(1), 5108-5108 (2019-11-11)
Mounting evidence suggests that the tumor microenvironment is profoundly immunosuppressive. Thus, mitigating tumor immunosuppression is crucial for inducing sustained antitumor immunity. Whereas previous studies involved intratumoral injection, we report here an inhalable nanoparticle-immunotherapy system targeting pulmonary antigen presenting cells (APCs)

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