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840046P

Avanti

Brain PI(4,5)P2

Avanti Research - A Croda Brand

Synonyme(s) :

Brain PI(4,5)P2

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About This Item

Numéro CAS:
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Description

L-α-phosphatidylinositol-4,5-bisphosphate (Brain, Porcine) (ammonium salt)

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 1 mg (840046P-1mg)
pkg of 1 × 10 mg (840046P-10mg)
pkg of 1 × 25 mg (840046P-25mg)
pkg of 1 × 5 mg (840046P-5mg)

Fabricant/nom de marque

Avanti Research - A Croda Brand

Type de lipide

phosphoglycerides

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

[H][C@@](COP(O[C@H]1[C@H](O)[C@@H](OP([O-])(O)=O)[C@H](OP(O)([O-])=O)[C@@H](O)[C@H]1O)([O-])=O)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O.[NH4+].[NH4+].[NH4+]

InChI

1S/C47H85O19P3.3H3N/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-41(49)63-39(37-61-40(48)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2)38-62-69(59,60)66-45-42(50)43(51)46(64-67(53,54)55)47(44(45)52)65-68(56,57)58;;;/h11,13,17,19,22,24,28,30,39,42-47,50-52H,3-10,12,14-16,18,20-21,23,25-27,29,31-38H2,1-2H3,(H,59,60)(H2,53,54,55)(H2,56,57,58);3*1H3/b13-11-,19-17-,24-22-,30-28-;;;/t39-,42?,43+,44?,45-,46?,47?;;;/m1.../s1

Clé InChI

GAIOWTITBYPFJE-JVILRMJCSA-N

Catégories apparentées

Description générale

Although PI(4,5)P2 is a minor component of cell membranes, it plays a critical role as a substrate for a number of important signaling proteins. PI(4,5)P2 is an intermediate in the IP3/DAG pathway where it is hydrolyzed by phospholipase C to liberate the second messengers, inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). PI(4,5)P2 is also a substrate for PI 3-kinase where it is phosphorylated to PI(3,4,5)P3, an activator of downstream signaling components such as the protein kinase AKT.
Phosphatidylinositol 4,5-bisphosphate (PIP2) is synthesized from the precursor phosphatidylinositol 4-phosphate(PI4P). PIP2 is a phosphoinositide with three negative charges.

Application

Brain PI(4,5)P2 has been used:
  • in the preparation of Folch liposome
  • in the preparation of giant unilamellar vesicles and multilamellar lipid sheets
  • as a substrate for rubidium flux assay
  • in the biochemical reaction assay mixture for various lipid kinases like Phosphatidylinositol-3-kinase gamma (PI3Kγ), Phosphatidylinositol-3-kinase beta (PI3Kβ), Phosphatidylinositol-3-kinase gamma (PI3Kα)

Actions biochimiques/physiologiques

Phosphatidylinositol 4,5-bisphosphate (PIP2) is a signaling phospholipid, present in the plasma membrane. It acts as a precursor for inositide 3 phosphate, diacylglycerol. PIP2 is a gating ligand for most of the ion channels. It functions as an activatory ligand for eukaryotic inward rectifier potassium (Kir) channels.

Conditionnement

5 mL Clear Glass Sealed Ampule (840046P-10mg)
5 mL Clear Glass Sealed Ampule (840046P-1mg)
5 mL Clear Glass Sealed Ampule (840046P-25mg)
5 mL Clear Glass Sealed Ampule (840046P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Souvent commandé avec ce produit

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3


Certificats d'analyse (COA)

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Structural dynamics of potassium-channel gating revealed by single-molecule FRET
Wang S, et al.
Nature Structural and Molecular Biology, 23(1), 31-31 (2016)
Friction mediates scission of tubular membranes scaffolded by BAR proteins
Simunovic M, et al.
Cell, 170(1), 172-184 (2017)
Membrane fission is promoted by insertion of amphipathic helices and is restricted by crescent BAR domains
Boucrot E, et al.
Cell, 149(1), 124-136 (2012)
Regulation of ion channels by phosphatidylinositol 4, 5-bisphosphate
Suh BC and Hille B
Current Opinion in Neurobiology, 15(3), 370-378 (2005)
Rose E Dixon et al.
eLife, 4 (2015-02-26)
In the heart, reliable activation of Ca(2+) release from the sarcoplasmic reticulum during the plateau of the ventricular action potential requires synchronous opening of multiple CaV1.2 channels. Yet the mechanisms that coordinate this simultaneous opening during every heartbeat are unclear.

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