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840033P

Avanti

14:0 PS

Avanti Research - A Croda Brand

Synonyme(s) :

1,2-ditetradecanoyl-sn-glycero-3-phospho-L-serine (sodium salt); DMPS; PS(14:0/14:0)

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About This Item

Formule empirique (notation de Hill):
C34H65NO10PNa
Numéro CAS:
Poids moléculaire :
701.84
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Description

1,2-dimyristoyl-sn-glycero-3-phospho-L-serine (sodium salt)

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 10 mg (840033P-10mg)
pkg of 1 × 200 mg (840033P-200mg)
pkg of 1 × 25 mg (840033P-25mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand

Type de lipide

phospholipids
cardiolipins

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(OC[C@](C([O-])=O)([H])[NH3+])=O)(OC(CCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C34H66NO10P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-32(36)42-27-30(28-43-46(40,41)44-29-31(35)34(38)39)45-33(37)26-24-22-20-18-16-14-12-10-8-6-4-2;/h30-31H,3-29,35H2,1-2H3,(H,38,39)(H,40,41);/q;+1/p-1/t30-,31+;/m1./s1

Clé InChI

QSHQBWBFNCFHLO-MFABWLECSA-M

Description générale

Phosphatidylserine (PS) is a retinal phospholipid, which carries long-chain highly unsaturated fatty acyl groups.

Application

14:0 PS may be used as an internal standard for spiking serum lipid samples for liquid chromatography-mass spectroscopy analysis and as a component in the phospholipid monolayer to mimic model cancer cell membrane for the anticancer drug doxorubicin (DOx) interaction studies. It has been used in lipid binding assay to assess the binding of monoclonal antibodies (mAbs).

Actions biochimiques/physiologiques

Phosphatidylserine (PS) helps to activate protein kinase C (PKC). It may possess anti-inflammatory properties. PS is also known to participate in tyrosine hydroxylase activation. It is also involved in the uptake of Ca2+ and glucose.

Conditionnement

5 mL Amber Glass Screw Cap Vial (840033P-10mg)
5 mL Amber Glass Screw Cap Vial (840033P-200mg)
5 mL Amber Glass Screw Cap Vial (840033P-25mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Cognitive Effects of Nutraceuticals
Nutraceuticals, 29-48 (2016)
B Fichtl et al.
Langmuir : the ACS journal of surfaces and colloids, 34(16), 4914-4919 (2018-04-04)
Currently, biological signaling is envisaged as a combination of activation and movement, triggered by local molecular interactions and molecular diffusion, respectively. However, here, we suggest that other fundamental physical mechanisms might play an at least equally important role. We have
Effect of pH on the interactions of doxorubicin with charged lipid monolayers containing 1,2-dimyristoyl-sn-glycero-3-phospho-l-serine - An important component of cancer cell membranes
Matyszewska D, et al.
Electrochimica Acta, 280, 229-237 (2018)
BIOSYNTHESIS OF MEMBRANE LIPIDS IN THE RETINA: SUBCELLULAR DISTRIBUTION AND PROPRANOLOL ACTION ON PHOSPHATIDIC ACID, PHOSPHATIDYLSERINE AND PHOSPHATIDYLETHANOLAMINE
Neurochemistry of the Retina, 17-28 (1980)
Charles F DeLisle et al.
The FEBS journal (2020-02-23)
Pro-islet amyloid polypeptide (proIAPP) is the prohormone precursor molecule to IAPP, also known as amylin. IAPP is a calcitonin family peptide hormone that is cosecreted with insulin, and largely responsible for hunger satiation and metabolic homeostasis. Amyloid plaques containing mixtures

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