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890704C

Avanti

18:1 EPC (Cl Salt)

Avanti Research - A Croda Brand 890704C

Synonim(y):

1,2-dioleoyl-sn-glycero-3-ethylphosphocholine (chloride salt)

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About This Item

Wzór empiryczny (zapis Hilla):
C46H89NO8PCl
Numer CAS:
Masa cząsteczkowa:
850.63
Kod UNSPSC:
12352211
NACRES:
NA.25

Postać

liquid

opakowanie

pkg of 1 × 2.5 mL (890704C-25mg)
pkg of 1 × 4 mL (890704C-100mg)
pkg of 2 × 4 mL (890704C-200mg)

producent / nazwa handlowa

Avanti Research - A Croda Brand 890704C

stężenie

10 mg/mL (890704C-25mg)
25 mg/mL (890704C-100mg)
25 mg/mL (890704C-200mg)

typ lipidu

transfection
cationic lipids

Warunki transportu

dry ice

temp. przechowywania

−20°C

ciąg SMILES

O=P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O)OCC.[Cl-]

Opis ogólny

1,2-dioleoyl-sn-glycero-3-ethylphosphocholine (18:1 EPC) is a cationic alkylated phospholipid.

Zastosowanie

1,2-dioleoyl-sn-glycero-3-ethylphosphocholine (chloride salt) (18:1 EPC (Cl Salt)) is suitable:
  • for composing lipid shell to prepare lipopolyplex/mRNA vaccine
  • in solvent-assisted preparation of supported lipid bilayers
  • along with 1,2-dioleoyl-sn-glycero-3-phosphatidylethanolamine (DOPE) in mixed liposomes as colloidal vectors for physicochemical study of the DNA compaction
  • to formulate the lipid nanoparticle (LNP1) to enhance intracellular delivery mediated by shock waves

Działania biochem./fizjol.

1,2-dioleoyl-sn-glycero-3-ethylphosphocholine (18:1 EPC) serves as a transfection reagent. 18:1 EPC is applicable in liposomes and lipoplexes. It is a potential vector in gene therapy.

Opakowanie

5 mL Clear Glass Sealed Ampule (890704C-100mg)
5 mL Clear Glass Sealed Ampule (890704C-200mg)
5 mL Clear Glass Sealed Ampule (890704C-25mg)

Informacje prawne

Avanti Research is a trademark of Avanti Polar Lipids, LLC
This page may contain text that has been machine translated.

Piktogramy

Skull and crossbonesHealth hazard

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3

Organy docelowe

Liver,Kidney, Respiratory system

Kod klasy składowania

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

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


Certyfikaty analizy (CoA)

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Gene vectors based on DOEPC/DOPE mixed cationic liposomes: a physicochemical study
Munoz U, et al.
Soft Matter, 7(13), 5991-6004 (2011)
Stefano Persano et al.
Biomaterials, 125, 81-89 (2017-02-24)
mRNA-based vaccines have the benefit of triggering robust anti-cancer immunity without the potential danger of genome integration from DNA vaccines or the limitation of antigen selection from peptide vaccines. Yet, a conventional mRNA vaccine comprising of condensed mRNA molecules in
Abdul Rahim Ferhan et al.
Nature protocols, 14(7), 2091-2118 (2019-06-09)
The supported lipid bilayer (SLB) platform is a popular cell membrane mimic that is utilized in the chemical, biological, materials science, and medical fields. To date, SLB preparation has proven challenging because of the need for specialized fabrication equipment, domain-specific
Jing Zhang et al.
ACS applied materials & interfaces, 11(11), 10481-10491 (2019-02-23)
Cellular membranes are, in general, impermeable to macromolecules (herein referred to as macrodrugs, e.g., recombinant protein, expression plasmids, or mRNA), which is a major barrier for clinical translation of macrodrug-based therapies. Encapsulation of macromolecules in lipid nanoparticles (LNPs) can protect
Kabir H Biswas et al.
Langmuir : the ACS journal of surfaces and colloids, 34(4), 1775-1782 (2017-12-28)
The pathway of vesicle adsorption onto a solid support depends on the material composition of the underlying support, and there is significant interest in developing material-independent strategies to modulate the spectrum of vesicle-substrate interactions on a particular surface. Herein, using

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