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       Category : Phosphoinositide Reagents and Derivatives : Phosphoinositide (PI & PIP) reagents, synthetic :   PIP3, PI(3,4,5)P3, Phosphatidylinositol 3,4,5-tris : PtdIns(3,4,5)P3 diC16, D-myo-Phosphatidylinositol 3,4,5-trisphosphate



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Product Name

Catalog Number

Unit Price
Phosphatidylinositol(3,4,5) trisphosphate diC16, also known as: PtdIns(3,4,5)P3, PI(3,4,5)P3 or PIP3

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 3,4,5-trisphosphate (PtdIns(3,4,5)P3)D (+)-sn-1,2-di-O-hexadecanoylglyceryl, 3-O-phospho linked [165689-82-7]
Molecular weight:
—1204.84
Molecular Formula:
— C41H75Na7O22P4
Storage:
—-20 °C
Applications:
—Assay development-Immunofluorescence- Determine lipid-protein interaction
Technical Questions:
—Phosphoinositide Reagents
Featured in Publication:
—AJP - Renal Physiology, Apr 2006
—AJP - Lung Cellular and Molecular Physiol, Mar 2006
Catalog:
—Phosphoinositide (PI & PIP) reagents, synthetic
 
Additional Informaiton
  --
 PIP FAQ's
  --
 P-3916 Sodium Salt
  --
 P-3916 Ammonium Salt
 
 
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