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       Category : Phosphoinositide Reagents and Derivatives : Phosphoinositide (PI & PIP) reagents, synthetic :   PI(4,5)P2, Phosphatidylinositol 4,5-bisphosphate : Phosphatidylinositol(4,5) bisphosphate diC16, PtdIns(4,5)P2, PI(4,5)P2



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Product Name

Catalog Number

Unit Price
Phosphatidylinositol(4,5) bisphosphate diC16, also known as: PtdIns(4,5)P2, PI(4,5)P2 or PIP2

Bulk discounts available, please email echelon@echelon-inc.com for information.

Phosphoinositides are synthesized from naturally-occurring chiral precursors. The inositol head groups are derived from methyl a-D-glucopyranoside via a Ferrier rearrangement; the diacylglyceryl moieties are prepared from (+)-isopropylideneglycerol. Each compound is provided as a lyophilized powder as the sodium salt. Ammonium salts are also available on request as a custom order at the same price. The isomeric purity is >95% for the phosphate position(s) indicated. Long chain phosphoinositides, including our di-C16 fatty acid products whose product numbers end in 16, are quite insoluble in aqueous solutions and may require vortex mixing, brief water-bath sonication, heating and/or addtion of some organic solvent for complete dissolution. Our diC8 products, whose product numbers end in 08, are soluble in water at 1mg/ml.
Benefits:
—Isomericly pure- Widest selection of PIPs and related products- Used in hundreds of publications
Chemical Name:
—D-myo-Phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2)D (+)-sn-1,2-di-O-hexadecanoylglyceryl, 3-O-phospho linked, [120595-88-2]
Molecular weight:
—1080.9
Molecular Formula:
— C41H76Na5O19P3
Storage:
—-20 °C
Applications:
—Assay development-Immunofluorescence- Determine lipid-protein interaction
Featured in Publication:
—AJP - Cell Physiology, May 2006
—AJP - Lung Cellular and Molecular Physiology, Mar 2006
Technical Questions:
—Phosphoinositide Reagents
Catalog:
—Phosphoinositide (PI & PIP) reagents, synthetic
 
Additional Informaiton
  --
 PIP FAQ's
  --
 P-4516 TDS
 
 
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