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850141P

Avanti

16:0 PI

1,2-dipalmitoyl-sn-glycero-3-phospho-(1′-myo-inositol) (ammonium salt), powder

Synonyme(s) :

1,2-dihexadecanoyl-sn-glycero-3-phospho-(1′-myo-inositol) (ammonium salt); PI(16:0/16:0); DPPI; 110657

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About This Item

Formule empirique (notation de Hill):
C41H82NO13P
Numéro CAS:
Poids moléculaire :
828.06
Code UNSPSC :
51191904
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 100 μg (with stopper and crimp cap (850141P-100ug))
pkg of 1 × 500 μg (with stopper and crimp cap (850141P-500ug))

Fabricant/nom de marque

Avanti Research - A Croda Brand 850141P

Type de lipide

phospholipids
cardiolipins

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[NH4+]

Description générale

Inositol phospholipid species are membrane-bound signaling molecules that have been implicated in almost all aspects of cellular physiology, including cellular growth, metabolism, proliferation, and survival.
Phosphatidylinositol (PtdIns) is a structural phospholipid. PI is synthesized by mycobacteria and other bacterial genera in prokaryotes.

Application

16:0 PI has been used as internal lipid standard for matrix-assisted laser desorption/ionization (MALDI)- fourier-transform ion cyclotron resonance (FTICR)- mass spectrometry (MS) and analysis. It is also suitable for use as an internal standard for mass spectrometric analyses.

Actions biochimiques/physiologiques

Phosphatidylinositol (PI) participates in polyphosphoinositide turnover. It can be used as a substrate to produce several molecules, that can modulate various cellular functions. In eukaryotes, phosphatidylinositol (PI)-based lipids (phosphoinositides) plays a key role in intracellular signalling. It is also involved in the anchoring of glycosylphosphatidylinositol-linked proteins to the membrane.

Conditionnement

2 mL Amber Serum Vial with Stopper and Crimp Cap (850141P-100ug)
2 mL Amber Serum Vial with Stopper and Crimp Cap (850141P-500ug)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids


Certificats d'analyse (COA)

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Les clients ont également consulté

Phosphatidylinositol 4-Kinase from Bovine Brain
Methods in Neurosciences, 18, 93-99 (1993)
Phosphatidylinositol Turnover and Receptors
reference module in biomedical sciences (2016)
Metabolic Heavy Isotope Labeling to Study Glycerophospholipid Homeostasis of Cultured Cells
Hanninen S, et al.
Bio-protocol, 7(9) (2017)
Structural basis for phosphatidylinositol-phosphate biosynthesis
Clarke OB, et al.
Nature Communications, 6, 8505-8505 (2015)
Jakub Suchodolski et al.
Yeast (Chichester, England), 37(1), 117-129 (2019-12-12)
Adherence of the fungus, Candida albicans, to biotic (e.g. human tissues) and abiotic (e.g. catheters) surfaces can lead to emergence of opportunistic infections in humans. The process of adhesion and further biofilm development depends, in part, on cell surface hydrophobicity

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